Organic electrolytic solution and lithium battery including the same

ABSTRACT

An organic electrolytic solution includes a first lithium salt; an organic solvent; a bicyclic sulfate-based compound represented by Formula 1 below; and a monocyclic phosphate-based compound represented by Formula K1 below:wherein in Formula 1, each of A1, A2, A3, and A4 is independently a covalent bond, a substituted or unsubstituted C1-C5 alkylene group, a carbonyl group, or a sulfinyl group, wherein both A1 and A2 are not a covalent bond and both A3 and A4 are not a covalent bond, and in Formula K1, each of A5 and A6 is independently a substituted or unsubstituted C1-C5 alkylene group.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part of U.S. patent applicationSer. No. 16/135,301 filed Sep. 19, 2018, which is a continuation-in-partof U.S. patent application Ser. No. 15/422,873, filed on Feb. 2, 2017,both entitled “Lithium Battery” which are hereby incorporated byreference in their entirety. Korean Patent Application No.10-2016-0016352, filed on Feb. 12, 2016, in the Korean IntellectualProperty Office, and entitled: “Lithium Battery,” is incorporated byreference herein in its entirety.

BACKGROUND 1. Field

Embodiments relate to organic electrolytic solutions and lithiumbatteries including the same.

2. Description of the Related Art

Lithium batteries are used as driving power sources for portableelectronic devices, including video cameras, mobile phones, notebookcomputers, and the like. Lithium secondary batteries are rechargeable athigh rates and have an energy density per unit weight that is at leastthree times as large as that of existing lead storage batteries,nickel-cadmium batteries, nickel-hydrogen batteries, or nickel-zincbatteries.

SUMMARY

Embodiments include organic electrolytic solutions including additivesfor electrolytes of lithium batteries.

Embodiments include lithium batteries including the organic electrolyticsolutions.

Embodiments are directed to an organic electrolytic solution including afirst lithium salt, an organic solvent, a bicyclic sulfate-basedcompound represented by Formula 1 below, and a monocyclicphosphate-based compound represented by Formula K1 below:

wherein, in Formula 1, each of A₁, A₂, A₃, and A₄ is independently acovalent bond, a substituted or unsubstituted C₁-C₅ alkylene group, acarbonyl group, or a sulfinyl group, wherein both A₁ and A₂ are not acovalent bond and both A₃ and A₄ are not a covalent bond, and

each of A₅ and A₆ is independently a substituted or unsubstituted C₁-C₅alkylene group.

At least one of A₁, A₂, A₃, and A₄ may be an unsubstituted orsubstituted C₁-C₅ alkylene group, wherein a substituent of thesubstituted C₁-C₅ alkylene group is at least one selected from ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom, and

at least one of A₅ and A₆ is an unsubstituted or substituted C₁-C₅alkylene group, wherein a substituent of the substituted C₁-C₅ alkylenegroup is a halogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom.

At least one of A₁, A₂, A₃, and A₄ may be an unsubstituted orsubstituted C₁-C₅ alkylene group, wherein a substituent of thesubstituted C₁-C₅ alkylene group is a halogen, a methyl group, an ethylgroup, a propyl group, an isopropyl group, a butyl group, a tert-butylgroup, a trifluoromethyl group, a tetrafluoroethyl group, a phenylgroup, a naphthyl group, a tetrafluorophenyl group, a pyrrolyl group, ora pyridinyl group, and

at least one of A₅ and A₆ is a substituted C₁-C₅ alkylene group, whereina substituent of the substituted C₁-C₅ alkylene group is a halogen, amethyl group, an ethyl group, a propyl group, an isopropyl group, abutyl group, a tert-butyl group, a monofluoromethyl group, adifluoromethyl group, a trifluoromethyl group, or a tetrafluoroethylgroup.

The substituted C₁-C₅ alkylene group may be substituted with a polarfunctional group including at least one heteroatom, wherein the polarfunctional group is —F, —Cl, —Br, —I, —CN, —N═C═S, —(CH₂CH₂O)_(n)—R¹² (nis an integer of 1 to 10), —C(═O)OR¹⁶, —OR¹⁶, —OC(═O)OR¹⁶,—R¹⁵OC(═O)OR¹⁶, —C(═O)R¹⁶, —R¹⁵C(═O)R¹⁶, —OC(═O)R¹⁶, —R¹⁵OC(═O)R¹⁶,—C(═O)—O—C(═O)R¹⁶, —R¹⁵C(═O)—O—C(═O)R¹⁶, —SR¹⁶, —R¹⁵SR¹⁶, —SSR¹⁶,—R¹⁵SSR¹⁶, —S(═O)R¹⁶, —R¹⁵S(═O)R¹⁶, —R¹⁵C(═S)R¹⁶, —R¹⁵C(═S)SR¹⁶,—R¹⁵SO₃R¹⁶, —SO₃R¹⁶, —NNC(═S)R¹⁶, —R¹⁵NNC(═S)R¹⁶, —R¹⁵N═C═S, —NCO,—R¹⁵—NCO, —NO₂, —R¹⁵NO₂, —R¹⁵SO₂R¹⁶, —SO₂R¹⁶,

wherein, in the formulae above, each of R¹¹ and R¹⁵ is independently ahalogen-substituted or unsubstituted C₁-C₂₀ alkylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynylene group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkylene group, ahalogen-substituted or unsubstituted C₆-C₄₀ arylene group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroarylene group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylarylene group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkylene group; and eachof R¹², R¹³, R¹⁴ and R¹⁶ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ trialkylsilyl group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkyl group.

The bicyclic sulfate-based compound may be represented by Formula 2 or3:

wherein, in Formulae 2 and 3, each of B₁, B₂, B₃, B₄, D₁, and D₂ isindependently —C(E₁)(E₂)-, a carbonyl group, or a sulfinyl group; andeach of E₁ and E₂ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

Each of E₁ and E₂ may be independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₁₀ alkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

Each of E₁ and E₂ may be independently hydrogen, fluorine (F), chlorine(Cl), bromine (Br), iodine (I), a methyl group, an ethyl group, a propylgroup, an isopropyl group, a butyl group, a tert-butyl group, atrifluoromethyl group, a tetrafluoroethyl group, a phenyl group, anaphthyl group, a tetrafluorophenyl group, a pyrrolyl group, or apyridinyl group.

The bicyclic sulfate-based compound may be represented by Formula 4 or5:

wherein, in Formulae 4 and 5, each of R₁, R₂, R₃, R₄, R₂₁, R₂₂, R₂₃,R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

Each of R₁, R₂, R₃, R₄, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ maybe independently hydrogen, F, Cl, Br, I, a methyl group, an ethyl group,a propyl group, an isopropyl group, a butyl group, a tert-butyl group, atrifluoromethyl group, a tetrafluoroethyl group, a phenyl group, anaphthyl group, a tetrafluorophenyl group, a pyrrolyl group, or apyridinyl group.

The bicyclic sulfate-based compound may be represented by one ofFormulae 6 to 17 below:

The monocyclic phosphate-based compound represented by Formula K1 may berepresented by Formula K2 below:

wherein, in Formula K2, each of R₂₉, R₃₀, R₃₁, and R₃₂ is independentlyhydrogen, halogen, a halogen-substituted or unsubstituted C₁-C₂₀ alkylgroup, or a polar functional group containing a heteroatom, wherein thepolar functional group containing a heteroatom is —CN, —N═C═O, —N═C═S,—(CH₂CH₂O)_(n)—CH₃ (n is an integer of 1 to 10), —OS(═O)₂F, —OS(═O)₂CH₃,—OS(═O)₂CH₂CH₃, or —OS(═O)₂CF₃.

The monocyclic phosphate-based compound represented by Formula K1 may berepresented by one of Formulae K3 to K14 below:

An amount of the bicyclic sulfate-based compound may be from about 0.4wt % to about 5 wt % based on a total weight of the organic electrolyticsolution.

An amount of the monocyclic phosphate-based compound may be from about0.05 wt % to about 5 wt % based on the total weight of the organicelectrolytic solution.

The first lithium salt in the organic electrolytic solution may includeat least one selected from LiPF₆, LiBF₄, LiSbF₆, LiAsF₆, LiClO₄,LiCF₃SO₃, Li(CF₃SO₂)₂N, LiC₄F₉SO₃, LiAlO₂, LiAlCl₄,LiN(C_(x)F_(2x+1)SO₂)(C_(y)F_(2y+1)SO₂) where 2≤x≤20 and 2≤y≤20, LiCl,and LiI.

The organic electrolytic solution may further include a cyclic carbonatecompound, wherein the cyclic carbonate compound is vinylene carbonate(VC), VC substituted with a halogen, a cyano (CN) group, or a nitrogroup (NO₂), vinylethylene carbonate (VEC), VEC substituted with ahalogen, CN, or NO₂, fluoroethylene carbonate (FEC), or FEC substitutedwith a halogen, CN, or NO₂.

An amount of the cyclic carbonate compound may be from about 0.01 wt %to about 5 wt % based on a total weight of the organic electrolyticsolution.

The organic electrolytic solution may further include a second lithiumsalt different from the first lithium salt and represented by one ofFormulae 18 to 25 below:

An amount of the second lithium salt may be from about 0.1 wt % to about5 wt % based on a total weight of the organic electrolytic solution.

Embodiments are directed to a lithium battery including a cathodeincluding a cathode active material; an anode including an anode activematerial; and the organic electrolytic solution between the cathode andthe anode.

The cathode active material includes a nickel-containing layered lithiumtransition metal oxide, wherein a content of nickel in the lithiumtransition metal oxide is about 60 mol % or more with respect to a totalnumber of moles of transition metals.

The lithium transition metal oxide may be represented by Formula 26below:

Li_(a)Ni_(x)Co_(y)M_(z)O_(2-b)A_(b)  <Formula 26>

wherein, in Formula 26, 1.0≤a≤1.2, 0≤b≤0.2, 0.6≤x<1, 0<y≤0.2, 0<z≤0.2,and x+y+z=1. M may be at least one selected from manganese (Mn),vanadium (V), magnesium (Mg), gallium (Ga), silicon (Si), tungsten (W),molybdenum (Mo), iron (Fe), chromium (Cr), copper (Cu), zinc (Zn),titanium (Ti), aluminum (Al), and boron (B). A may be fluorine (F),sulfur (S), chlorine (Cl), bromine (Br), or a combination thereof.

The lithium transition metal oxide may be a compound represented byFormula 27 or 28 below:

LiNi_(x)Co_(y)Mn_(z)O₂  <Formula 27>

LiNi_(x)Co_(y)Al_(z)O₂,  <Formula 28>

wherein, in Formulae 27 and 28, 0.6≤x≤0.95, 0<y≤0.2, 0<z≤0.2, andx+y+z=1.

The lithium battery may have a high voltage of about 3.8 V or higher.

BRIEF DESCRIPTION OF THE DRAWINGS

Features will become apparent to those of skill in the art by describingin detail exemplary embodiments with reference to the attached drawingsin which:

FIG. 1 illustrates a graph showing discharge capacities at roomtemperature of lithium batteries manufactured according to Examples 4and 5 and Comparative Example 2;

FIG. 2 illustrates a graph showing capacity retention ratios at roomtemperature of the lithium batteries of Examples 4 and 5 and ComparativeExample 2;

FIG. 3 illustrates a graph showing discharge capacities at a hightemperature of the lithium batteries of Examples 4 and 5 and ComparativeExample 2;

FIG. 4 illustrates a graph showing capacity retention ratios at a hightemperature of the lithium batteries of Examples 4 and 5 and ComparativeExample 2;

FIG. 5 illustrates a graph showing capacity retention ratios at roomtemperature of the lithium batteries of Example 4 and ComparativeExample 2;

FIG. 6 illustrates a graph showing capacity retention ratios at a hightemperature of the lithium batteries of Example 4 and ComparativeExample 2; and

FIG. 7 illustrates a view of a lithium battery according to anembodiment.

DETAILED DESCRIPTION

Example embodiments will now be described more fully hereinafter withreference to the accompanying drawings; however, they may be embodied indifferent forms and should not be construed as limited to theembodiments set forth herein. Rather, these embodiments are provided sothat this disclosure will be thorough and complete, and will fullyconvey exemplary implementations to those skilled in the art.

In the drawing figures, the dimensions of layers and regions may beexaggerated for clarity of illustration. It will also be understood thatwhen a layer or element is referred to as being “on” another layer orelement, it can be directly on the other layer or element, orintervening layers may also be present. Further, it will be understoodthat when a layer is referred to as being “under” another layer, it canbe directly under, and one or more intervening layers may also bepresent. In addition, it will also be understood that when a layer isreferred to as being “between” two layers, it can be the only layerbetween the two layers, or one or more intervening layers may also bepresent. Like reference numerals refer to like elements throughout. Asused herein, the term “or” is not an exclusive term, e.g., “A or B”would include A, B, or A and B.

Hereinafter, an organic electrolytic solution according to exampleembodiments and a lithium battery including the organic electrolyticsolution will be described in detail.

An organic electrolytic solution according to an embodiment may include:a first lithium salt; an organic solvent; a bicyclic sulfate-basedcompound represented by Formula 1 below; and a monocyclicphosphate-based compound represented by Formula K1 below:

wherein, in Formula 1, each of A₁, A₂, A₃, and A₄ may be independently acovalent bond, a substituted or unsubstituted C₁-C₅ alkylene group, acarbonyl group, or a sulfinyl group, in which both A₁ and A₂ are not acovalent bond and both A₃ and A₄ are not a covalent bond, and each of A₅and A₆ may be independently a substituted or unsubstituted C₁-C₅alkylene group.

The organic electrolytic solution as additives for a lithium battery,including both the bicyclic sulfate-based compound and the monocyclicphosphate-based compound, may enhance battery performance, such ashigh-temperature characteristics, lifespan characteristics, or the like.

The bicyclic sulfate-based compound may have a structure in which twosulfate rings are linked to each other in a spiro form.

Without being bound to any particular theory and for betterunderstanding, a reason for which the performance of a lithium batteryis improved by addition of the bicyclic sulfate-based compound to theelectrolytic solution will now be described in further detail.

When a bicyclic sulfate-based compound is included in the electrolyticsolution, a sulfate ester group of the bicyclic sulfate-based compoundmay be reduced by itself by accepting electrons from a surface of ananode during charging, or may react with a previously-reduced polarsolvent molecule, thereby affecting characteristics of an SEI layerformed at the surface of the anode. For example, the bicyclicsulfate-based compound including the sulfate ester group may more easilyaccept electrons from an anode, as compared to polar solvents. Forexample, the bicyclic sulfate-based compound may be reduced at a lowervoltage than a polar solvent before the polar solvent is reduced.

For example, the bicyclic sulfate-based compound includes a sulfateester group, and thus may be more easily reduced and/or decomposed intoradicals and/or ions during charging. Consequently, the radicals and/orions may bind with lithium ions to form an appropriate SEI layer on ananode, thereby preventing formation of a product obtained by furtherdecomposition of a solvent. The bicyclic sulfate-based compound may forma covalent bond with, for example, a carbonaceous anode itself or avariety of functional groups on the surface of the carbonaceous anode,or may be adsorbed onto the surface of an electrode. A modified SEIlayer with improved stability, formed by such binding and/or adsorption,may be more durable even after charging and discharging for a long timeperiod, as compared to an SEI layer formed from only an organic solvent.The durable modified SEI layer may in turn more effectively blockco-intercalation of the organic solvent solvating lithium ions duringintercalation of the lithium ions into an electrode. Accordingly, themodified SEI layer may more effectively block direct contact between theorganic solvent and an anode to further improve reversibility ofintercalation/deintercalation of lithium ions, resulting in an increasein discharge capacity and improvement of lifespan characteristics of thebattery fabricated.

Also, due to the inclusion of the sulfate ester group, the bicyclicsulfate-based compound may be coordinated on a surface of a cathode,thereby affecting characteristics of a protection layer formed on thesurface of the cathode. For example, the sulfate ester group may becoordinated to transition metal ions of a cathode active material toform a complex. This complex may form a modified protection layer withimproved stability that is more durable even after charging anddischarging for a long time period than a protection layer formed fromonly the organic solvent. In addition, the durable modified protectionlayer may more effectively block co-intercalation of the organic solventsolvating lithium ions during intercalation of the lithium ions into anelectrode. Accordingly, the modified protection layer may moreeffectively block direct contact between the organic solvent and thecathode to further improve the reversibility ofintercalation/deintercalation of lithium ions, resulting in increasedstability and improved lifespan characteristics of the batteryfabricated.

In addition, the bicyclic sulfate-based compound has a structure inwhich a plurality of rings are linked in a spiro form and thus has arelatively larger molecular weight than that of a general sulfate-basedcompound and accordingly, may be thermally stable.

For example, the bicyclic sulfate-based compound may form an SEI layerat a surface of an anode or a protection layer at a surface of a cathodeand may exhibit enhanced lifespan characteristics of the lithium batteryfabricated at a high temperature due to the improved thermal stability.

The monocyclic phosphate-based compound may help inhibit decompositionof lithium salts, inhibit a presence of hydrofluoric acid by reactingwith hydrofluoric acid (HF) generated in the organic electrolyticsolution, and suppress discoloration of the electrolytic solution. Thus,the monocyclic phosphate-based compound may help suppress side reactionswith the organic electrolytic solution.

When the organic electrolytic solution includes both the bicyclicsulfate-based compound and the monocyclic phosphate-based compound, in alithium battery, lifespan characteristics and thermal stability may befurther enhanced and gas generation may be more effectively suppressed.

In the bicyclic sulfate-based compound of Formula 1 above included inthe organic electrolytic solution, at least one of A₁, A₂, A₃, and A₄may be an unsubstituted or substituted C₁-C₅ alkylene group, and asubstituent of the substituted C₁-C₅ alkylene group may be ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom.

In the monocyclic phosphate-based compound represented by Formula K1included in the organic electrolytic solution, at least one of A₅ and A₆may be an unsubstituted or substituted C₁-C₅ alkylene group, and asubstituent of the substituted C₁-C₅ alkylene group may be ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom.

For example, at least one of A₁, A₂, A₃, and A₄ may be an unsubstitutedor substituted C₁-C₅ alkylene group, and a substituent of thesubstituted C₁-C₅ alkylene group may be a halogen, a methyl group, anethyl group, a propyl group, an isopropyl group, a butyl group, atert-butyl group, a trifluoromethyl group, a tetrafluoroethyl group, aphenyl group, a naphthyl group, a tetrafluorophenyl group, a pyrrolylgroup, or a pyridinyl group. For example, the substituent of thesubstituted C₁-C₅ alkylene group may be a suitable substituent foralkylene groups.

For example, at least one of A₅ and A₆ may be a substituted C₁-C₅alkylene group, and a substituent of the substituted C₁-C₅ alkylenegroup may be a halogen, a methyl group, an ethyl group, a propyl group,an isopropyl group, a butyl group, a tert-butyl group, amonofluoromethyl group, a difluoromethyl group, a trifluoromethyl group,or a tetrafluoroethyl group. For example, the substituent of thesubstituted C₁-C₅ alkylene group may be a suitable substituent availablefor alkylene groups used in the art.

In some implementations, in the bicyclic sulfate-based compound ofFormula 1 above and the monocyclic phosphate-based compound of FormulaK1, the substituent of the substituted C₁-C₅ alkylene group may be apolar functional group having a heteroatom. The heteroatom of the polarfunctional group may be at least one selected from oxygen, nitrogen,phosphorus, sulfur, silicon, and boron.

For example, the polar functional group having a heteroatom may be —F,—Cl, —Br, —I, —CN, —N═C═S, —(CH₂CH₂O)_(n)—R¹² in which n is an integerof 1 to 10, —C(═O)OR¹⁶, —OR¹⁶, —OC(═O)OR¹⁶, —R¹⁵OC(═O)OR¹⁶, —C(═O)R¹⁶,—R¹⁵C(═O)R¹⁶, —OC(═O)R¹⁶, —R¹⁵OC(═O)R¹⁶, —C(═O)—O—C(═O)R¹⁶,—R¹⁵C(═O)—O—C(═O)R¹⁶, —SR¹⁶, —R¹⁵SR¹⁶, —SSR¹⁶, —R¹⁵SSR¹⁶, —S(═O)R¹⁶,—R¹⁵S(═O)R¹⁶, —R¹⁵C(═S)R¹⁶, —R¹⁵C(═S)SR¹⁶, —R¹⁵SO₃R¹⁶, —SO₃R¹⁶,—NNC(═S)R¹⁶, —R¹⁵NNC(═S)R¹⁶, —R¹⁵N═C═S, —NCO, —R¹—NCO, —NO₂, —R¹⁵NO₂,—R¹⁵O₂R¹⁶, —SO₂R¹⁶,

In the above formulae, each of R¹¹ and R¹⁵ may be independently ahalogen-substituted or unsubstituted C₁-C₂₀ alkylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynylene group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkylene group, ahalogen-substituted or unsubstituted C₆-C₄₀ arylene group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroarylene group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylarylene group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkylene group. Each ofR¹², R¹³, R¹⁴ and R¹⁶ may be independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ trialkylsilyl group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkyl group.

For example, in the polar functional group having a heteroatom, ahalogen substituent of the alkyl group, the alkenyl group, the alkynylgroup, the cycloalkyl group, the aryl group, the heteroaryl group, thealkylaryl group, the trialkylsilyl group, or the aralkyl group may befluorine (F).

For example, the bicyclic sulfate-based compound included in the organicelectrolytic solution may be represented by Formula 2 or 3:

wherein, in Formulae 2 and 3, each of B₁, B₂, B₃, B₄, D₁, and D₂ may beindependently —C(E₁)(E₂)-, a carbonyl group, or a sulfinyl group. Eachof E₁ and E₂ may be independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

For example, each of E₁ and E₂ may be independently hydrogen, a halogen,a halogen-substituted or unsubstituted C₁-C₁₀ alkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

For example, each of E₁ and E₂ may be independently hydrogen, F,chlorine (Cl), bromine (Br), iodine (I), a methyl group, an ethyl group,a propyl group, an isopropyl group, a butyl group, a tert-butyl group, atrifluoromethyl group, a tetrafluoroethyl group, a phenyl group, anaphthyl group, a tetrafluorophenyl group, a pyrrolyl group, or apyridinyl group.

For example, each of E₁ and E₂ may be independently hydrogen, F, amethyl group, an ethyl group, a trifluoromethyl group, atetrafluoroethyl group, or a phenyl group.

For example, the bicyclic sulfate-based compound may be represented byFormula 4 or 5:

wherein, in Formulae 4 and 5, each of R₁, R₂, R₃, R₄, R₂₁, R₂₂, R₂₃,R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ may be independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.

For example, in Formulae 4 and 5 above, each of R₁, R₂, R₃, R₄, R₂₁,R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ may be independently hydrogen, F,Cl, Br, I, a methyl group, an ethyl group, a propyl group, an isopropylgroup, a butyl group, a tert-butyl group, a trifluoromethyl group, atetrafluoroethyl group, a phenyl group, a naphthyl group, atetrafluorophenyl group, a pyrrole group, or a pyridine group.

For example, in Formulae 4 and 5 above, each of R₁, R₂, R₃, R₄, R₂₁,R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ may be independently hydrogen, F,a methyl group, an ethyl group, a propyl group, a trifluoromethyl group,a tetrafluoroethyl group, or a phenyl group.

For example, the bicyclic sulfate-based compound may be represented byone of Formulae 6 to 17:

For example, the monocyclic phosphate-based compound may be representedby Formula K2 below:

wherein, in Formula K2, each of R₂₉, R₃₀, R₃₁, and R₃₂ may beindependently hydrogen, halogen, a halogen-substituted or unsubstitutedC₁-C₂₀ alkyl group, or a polar functional group containing a heteroatom,and the polar functional group containing a heteroatom is —CN, —N═C═O,—N═C═S, —(CH₂CH₂O)_(n)—CH₃ (in which n is an integer of 1 to 10),—OS(═O)₂F, —OS(═O)₂CH₃, —OS(═O)₂CH₂CH₃, or —OS(═O)₂CF₃.

For example, the monocyclic phosphate-based compound may be representedby one of Formulae K3 to K14:

As used herein, a and b of the expression “C_(a)-C_(b)” indicates thenumber of carbon atoms of a particular functional group. For example,the functional group may include a to b carbon atoms. For example, theexpression “C₁-C₄ alkyl group” indicates an alkyl group having 1 to 4carbon atoms, i.e., CH₃—, CH₃CH₂—, CH₃CH₂CH₂—, (CH₃)₂CH—, CH₃CH₂CH₂CH₂—,CH₃CH₂CH(CH₃)— and (CH₃)₃C—.

A particular radical may be called a mono-radical or a di-radicaldepending on the context. For example, when a substituent needs twobinding sites for binding with the rest of the molecule, the substituentmay be understood as a di-radical. For example, a substituent specifiedas an alkyl group that needs two binding sites may be a di-radical, suchas —CH₂—, —CH₂CH₂—, —CH₂CH(CH₃)CH₂—, or the like. The term “alkylene” asused herein indicates that the radical is a di-radical.

The terms “alkyl group” and “alkylene group” as used herein refer to abranched or unbranched aliphatic hydrocarbon group. In an embodiment,the alkyl group may be substituted or unsubstituted. Examples of thealkyl group include a methyl group, an ethyl group, a propyl group, anisopropyl group, a butyl group, an isobutyl group, a tert-butyl group, apentyl group, a hexyl group, a cyclopropyl group, a cyclopentyl group, acyclohexyl group, and a cycloheptyl group, each of which may beoptionally substituted or unsubstituted. In an embodiment, the alkylgroup may have 1 to 6 carbon atoms. For example, a C₁-C₆ alkyl group maybe methyl, ethyl, propyl, isopropyl, butyl, iso-butyl, sec-butyl,pentyl, 3-pentyl, hexyl, or the like.

The term “cycloalkyl group” as used herein refers to a fully saturatedcarbocyclic ring or ring system. For example, the cycloalkyl group maybe cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

The term “alkenyl group” as used herein refers to a hydrocarbon grouphaving 2 to 20 carbon atoms with at least one carbon-carbon double bond.examples of the alkenyl group include an ethenyl group, a 1-propenylgroup, a 2-propenyl group, a 2-methyl-1-propenyl group, a 1-butenylgroup, a 2-butenyl group, a cyclopropenyl group, a cyclopentenyl group,a cyclohexenyl group, and a cycloheptenyl group. In an embodiment, thesealkenyl groups may be substituted or unsubstituted. In an embodiment,the alkenyl group may have 2 to 40 carbon atoms.

The term “alkynyl group” as used herein refers to a hydrocarbon grouphaving 2 to 20 carbon atoms with at least one carbon-carbon triple bond.Examples of the alkynyl group include an ethynyl group, a 1-propynylgroup, a 1-butynyl group, and a 2-butynyl group. In an embodiment, thesealkynyl groups may be substituted or unsubstituted. In an embodiment,the alkynyl group may have 2 to 40 carbon atoms.

The term “aromatic” as used herein refers to a ring or ring system witha conjugated π electron system, and may refer to a carbocyclic aromaticgroup (e.g., a phenyl group) and a heterocyclic aromatic group (e.g.,pyridine). In this regard, an aromatic ring system as a whole mayinclude a monocyclic ring or a fused polycyclic ring (i.e., a ring thatshares adjacent atom pairs).

The term “aryl group” as used herein refers to an aromatic ring or ringsystem (i.e., a ring fused from at least two rings that shares twoadjacent carbon atoms) having only carbon atoms in its backbone. Whenthe aryl group is a ring system, each ring in the ring system isaromatic. Examples of the aryl group include a phenyl group, a biphenylgroup, a naphthyl group, a phenanthrenyl group, and naphthacenyl group.These aryl groups may be substituted or unsubstituted.

The term “heteroaryl group” as used herein refers to an aromatic ringsystem with one ring or plural fused rings, in which at least one ringatom is not carbon, i.e., a heteroatom. In the fused ring system, atleast one heteroatom may be present in only one ring. For example, theheteroatom may be oxygen, sulfur, or nitrogen. Examples of theheteroaryl group include a furanyl group, a thienyl group, an imidazolylgroup, a quinazolinyl group, a quinolinyl group, an isoquinolinyl group,a quinoxalinyl group, a pyridinyl group, a pyrrolyl group, an oxazolylgroup, and an indolyl group.

The terms “aralkyl group” and “alkylaryl group” as used herein refer toan aryl group linked as a substituent via an alkylene group, such as aC₇-C₁₄ aralkyl group. Examples of the aralkyl group or alkylaryl groupinclude a benzyl group, a 2-phenylethyl group, a 3-phenylpropyl group,and a naphthylalkyl group. In an embodiment, the alkylene group may be alower alkylene group (i.e., a C₁-C₄ alkylene group).

The term “cycloalkenyl group” as used herein refers to a non-aromaticcarbocyclic ring or ring system with at least one double bond. Forexample, the cycloalkenyl group may be a cyclohexenyl group.

The term “heterocyclic group” as used herein refers to a non-aromaticring or ring system having at least one heteroatom in its ring backbone.

The term “halogen” as used herein refers to a stable element belongingto Group 17 of the periodic table, for example, fluorine, chlorine,bromine, or iodine. For example, the halogen may be fluorine and/orchlorine.

In the present specification, a substituent may be derived bysubstitution of at least one hydrogen atom in an unsubstituted mothergroup with another atom or a functional group. Unless stated otherwise,the term “substituted” indicates that the above-listed functional groupsare substituted with at least one substituent selected from a C₁-C₄₀alkyl group, a C₂-C₄₀ alkenyl group, a C₃-C₄₀ cycloalkyl group, a C₃-C₄₀cycloalkenyl group, and a C₇-C₄₀ aryl group. The phrase “optionallysubstituted” as used herein indicates that the functional groupsdescribed above may be substituted with the aforementioned substituentsor may be unsubstituted.

The amount of the bicyclic sulfate-based compound of Formula 1 as anadditive in the organic electrolytic solution may range from about 0.4wt % to about 5 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the bicyclicsulfate-based compound of Formula 1 as an additive in the organicelectrolytic solution may range from about 0.4 wt % to about 3 wt %based on the total weight of the organic electrolytic solution. Forexample, the amount of the bicyclic sulfate-based compound of Formula 1in the organic electrolytic solution may range from about 0.6 wt % toabout 3 wt % based on the total weight of the organic electrolyticsolution. For example, the amount of the bicyclic sulfate-based compoundof Formula 1 in the organic electrolytic solution may be from about 0.7wt % to about 3 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the bicyclicsulfate-based compound of Formula 1 in the organic electrolytic solutionmay be from about 0.4 wt % to about 2.5 wt % based on the total weightof the organic electrolytic solution. For example, the amount of thebicyclic sulfate-based compound of Formula 1 in the organic electrolyticsolution may be from about 0.4 wt % to about 2 wt % based on the totalweight of the organic electrolytic solution. For example, the amount ofthe bicyclic sulfate-based compound of Formula 1 in the organicelectrolytic solution may be from about 0.4 wt % to about 1.5 wt % basedon the total weight of the organic electrolytic solution. When theamount of the bicyclic sulfate-based compound of Formula 1 is within theranges described above, further enhanced battery characteristics may beobtained.

The amount of the monocyclic phosphate-based compound of Formula K1 asan additive in the organic electrolytic solution may range from about0.05 wt % to about 5 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the monocyclicphosphate-based compound of Formula K1 as an additive in the organicelectrolytic solution may range from about 0.05 wt % to about 4 wt %based on the total weight of the organic electrolytic solution. Forexample, the amount of the monocyclic phosphate-based compound ofFormula K1 in the organic electrolytic solution may range from about0.05 wt % to about 3 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the monocyclicphosphate-based compound of Formula K1 in the organic electrolyticsolution may be from about 0.1 wt % to about 3 wt % based on the totalweight of the organic electrolytic solution. For example, the amount ofthe monocyclic phosphate-based compound of Formula K1 in the organicelectrolytic solution may be from about 0.4 wt % to about 3 wt % basedon the total weight of the organic electrolytic solution. For example,the amount of the monocyclic phosphate-based compound of Formula K1 inthe organic electrolytic solution may be from about 0.4 wt % to about2.5 wt % based on the total weight of the organic electrolytic solution.For example, the amount of the monocyclic phosphate-based compound ofFormula K1 in the organic electrolytic solution may be from about 0.4 wt% to about 2 wt % based on the total weight of the organic electrolyticsolution. For example, the amount of the monocyclic phosphate-basedcompound of Formula K1 in the organic electrolytic solution may be fromabout 0.4 wt % to about 1.5 wt % based on the total weight of theorganic electrolytic solution. When the amount of the monocyclicphosphate-based compound of Formula K1 is within the ranges describedabove, further enhanced battery characteristics may be obtained.

The first lithium salt included in the organic electrolytic solution mayinclude at least one selected from LiPF₆, LiBF₄, LiSbF₆, LiAsF₆, LiClO₄,LiCF₃SO₃, Li(CF₃SO₂)₂N, LiC₄F₉SO₃, LiAlO₂, LiAlCl₄,LiN(C_(x)F_(2x+1)SO₂)(C_(y)F_(2y+1)SO₂) where 2≤x≤20 and 2≤y≤20, LiCl,and LiI.

The concentration of the first lithium salt in the organic electrolyticsolution may be, for example, from about 0.01 M to about 2.0 M. Theconcentration of the first lithium salt in the organic electrolyticsolution may be appropriately adjusted as desired. When theconcentration of the first lithium salt is within the above range, abattery with further enhanced characteristics may be obtained.

The organic solvent included in the organic electrolytic solution may bea low-boiling point solvent. The term “low-boiling point solvent” refersto a solvent having a boiling point of 200° C. or less at 1 atmosphereat 25° C.

For example, the organic solvent may include at least one selected froma dialkyl carbonate, a cyclic carbonate, a linear or cyclic ester, alinear or cyclic amide, an alicyclic nitrile, a linear or cyclic ether,and derivatives thereof.

For example, the organic solvent may include at least one selected fromdimethyl carbonate (DMC), ethyl methyl carbonate (EMC), methyl propylcarbonate, ethyl propyl carbonate, diethyl carbonate (DEC), dipropylcarbonate, propylene carbonate (PC), ethylene carbonate (EC), butylenecarbonate, ethyl propionate, ethyl butyrate, acetonitrile,succinonitrile (SN), dimethyl sulfoxide, dimethylformamide,dimethylacetamide, γ-valerolactone, γ-butyrolactone, andtetrahydrofuran. For example, the organic solvent may be a suitablesolvent having a low-boiling point available in the art.

The organic electrolytic solution may further include other additives inaddition to the bicyclic sulfate-based compound. Due to the furtherinclusion of other additives, a lithium battery with further enhancedperformance may be obtained.

The additives further included in the organic electrolytic solution mayinclude a cyclic carbonate compound, a second lithium salt, or the like.

For example, the organic electrolytic solution may further include acyclic carbonate compound as an additive. The cyclic carbonate compoundused as an additive may be vinylene carbonate (VC), VC substituted witha halogen, a cyano (CN) group, or a nitro group (NO₂), vinyl ethylenecarbonate (VEC), VEC substituted with a halogen, CN, or NO₂,fluoroethylene carbonate (FEC), or FEC substituted with a halogen, CN,or NO₂. When the organic electrolytic solution further includes a cycliccarbonate compound as an additive, a lithium battery including theorganic electrolytic solution may have further enhanced charge anddischarge characteristics.

The amount of the cyclic carbonate compound in the organic electrolyticsolution may be, for example, from about 0.01 wt % to about 5 wt % basedon the total weight of the organic electrolytic solution. The amount ofthe cyclic carbonate compound may be appropriately adjusted as desired.For example, the amount of the cyclic carbonate compound in the organicelectrolytic solution may be from about 0.1 wt % to about 5 wt % basedon the total weight of the organic electrolytic solution. For example,the amount of the cyclic carbonate compound in the organic electrolyticsolution may be from about 0.1 wt % to about 4 wt % based on the totalweight of the organic electrolytic solution. For example, the amount ofthe cyclic carbonate compound in the organic electrolytic solution maybe from about 0.1 wt % to about 3 wt % based on the total weight of theorganic electrolytic solution. For example, the amount of the cycliccarbonate compound in the organic electrolytic solution may be fromabout 0.1 wt % to about 2 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the cyclic carbonatecompound in the organic electrolytic solution may be from about 0.2 wt %to about 2 wt % based on the total weight of the organic electrolyticsolution. For example, the amount of the cyclic carbonate compound inthe organic electrolytic solution may be from about 0.2 wt % to about1.5 wt % based on the total weight of the organic electrolytic solution.When the amount of the cyclic carbonate compound is within the aboveranges, a battery with further enhanced characteristics may be obtained.

For example, the organic electrolytic solution may further include asecond lithium salt as an additive. The second lithium salt isdistinguished from (i.e., different from) the first lithium salt. Ananion of the second lithium salt may be oxalate, PO₂F₂—, N(SO₂F)₂—, orthe like. For example, the second lithium salt may be a compoundrepresented by one of Formulae 18 to 25 below:

The amount of the second lithium salt in the organic electrolyticsolution may be from about 0.1 wt % to about 5 wt % based on the totalweight of the organic electrolytic solution. The amount of the secondlithium salt may be appropriately adjusted if desired. For example, theamount of the second lithium salt in the organic electrolytic solutionmay be from about 0.1 wt % to about 4.5 wt % based on the total weightof the organic electrolytic solution. For example, the amount of thesecond lithium salt in the organic electrolytic solution may be fromabout 0.1 wt % to about 4 wt % based on the total weight of the organicelectrolytic solution. For example, the amount of the second lithiumsalt in the organic electrolytic solution may be from about 0.1 wt % toabout 3 wt % based on the total weight of the organic electrolyticsolution. For example, the amount of the second lithium salt in theorganic electrolytic solution may be from about 0.1 wt % to about 2 wt %based on the total weight of the organic electrolytic solution. Forexample, the amount of the second lithium salt in the organicelectrolytic solution may be from about 0.2 wt % to about 2 wt % basedon the total weight of the organic electrolytic solution. For example,the amount of the second lithium salt in the organic electrolyticsolution may be from about 0.2 wt % to about 1.5 wt % based on the totalweight of the organic electrolytic solution. When the amount of thesecond lithium salt is within the above ranges, a battery with furtherenhanced characteristics may be obtained.

The organic electrolytic solution may be in a liquid or gel state. Theorganic electrolytic solution may be prepared by adding the firstlithium salt and the additive described above to the aforementionedorganic solvent.

A lithium battery according to another embodiment includes a cathodeincluding a cathode active material, an anode including an anode activematerial, and the above-described organic electrolytic solution betweenthe cathode and the anode.

Examples of the lithium battery include lithium secondary batteries suchas a lithium ion battery, a lithium ion polymer battery, a lithiumsulfur battery, or the like, and lithium primary batteries.

The cathode active material may include, for example, anickel-containing layered lithium transition metal oxide. The content ofnickel in the lithium transition metal oxide may be about 60 mol % ormore with respect to the total number of moles of transition metals.

The cathode active material may include a nickel-containing layeredlithium transition metal oxide, and the nickel-containing layeredlithium transition metal oxide may be represented by, for example,Formula 26 below:

Li_(a)Ni_(x)Co_(y)M_(z)O_(2-b)A_(b)  <Formula 26>

wherein, in Formula 26, 1.0≤a≤1.2, 0≤b≤0.2, 0.6≤x<1, 0<y≤0.2, 0<z≤0.2,and x+y+z=1; M is at least one selected from manganese (Mn), vanadium(V), magnesium (Mg), gallium (Ga), silicon (Si), tungsten (W),molybdenum (Mo), iron (Fe), chromium (Cr), copper (Cu), zinc (Zn),titanium (Ti), aluminum (Al), and boron (B); and A is fluorine (F),sulfur (S), chlorine (Cl), bromine (Br), or a combination thereof. Forexample, 0.7≤x<1, 0<y≤0.15, 0<z≤0.15, and x+y+z=1. For example,0.75≤x<1, 0<y≤0.125, 0<z≤0.125, and x+y+z=1. For example, 0.8≤x<1,0<y≤0.1, 0<z≤0.1, and x+y+z=1. For example, 0.85≤x<1, 0<y≤0.075,0<z≤0.075, and x+y+z=1.

The cathode active material includes a nickel-containing layered lithiumtransition metal oxide, and the nickel-containing layered lithiumtransition metal oxide may be represented by, for example, Formula 27 or28:

LiNi_(x)Co_(y)Mn_(z)O₂  <Formula 27>

LiNi_(x)Co_(y)Al_(z)O₂  <Formula 28>

wherein, in Formulae 27 and 28, 0.6≤x≤0.95, 0<y≤0.2, 0<z≤0.1, andx+y+z=1. For example, 0.7≤x≤0.95, 0<y≤0.15, 0<z≤0.15, and x+y+z=1. Forexample, 0.75≤x≤0.95, 0<y≤0.125, 0<z≤0.125, and x+y+z=1. For example,0.8≤x≤0.95, 0<y≤0.1, 0<z≤0.1, and x+y+z=1. For example, 0.85≤x≤0.95,0<y≤0.075, 0<z≤0.075, and x+y+z=1.

For example, in the lithium battery, the anode may include graphite. Forexample, the lithium battery may have a high voltage of about 3.80 V orhigher. For example, the lithium battery may have a high voltage ofabout 4.0 V or higher. For example, the lithium battery may have a highvoltage of about 4.35 V or higher.

For example, the lithium battery may be manufactured using the followingmethod.

A cathode may be prepared by a suitable method. For example, a cathodeactive material composition, in which the above-described cathode activematerial, a conductive material, a binder, and a solvent are mixed, maybe prepared. The cathode active material composition may be directlycoated onto a metal current collector, thereby completing themanufacture of a cathode plate. In some implementations, the cathodeactive material composition may be cast onto a separate support, and afilm separated from the support may be laminated onto a metal currentcollector, thereby completing the manufacture of a cathode plate.

For example, the cathode active material may be a compound representedby any one of Formulae: Li_(a)A_(1-b)B′_(b)D₂ where 0.90≤a≤1.8 and0≤b≤0.5; Li_(a)E_(1-b)B′_(b)O_(2-c)D_(c) where 0.90≤a≤1.8, 0≤b 0.5, and0≤c≤0.05; LiE_(2-b)B′_(b)O_(4-c)D_(c) where 0≤b≤0.5 and 0≤c≤0.05;Li_(a)Ni_(1-b-c)Co_(b)B′_(c)D_(α) where 0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05,and 0<α≤2; Li_(a)Ni_(1-b-c)Co_(b)B′_(c)O_(2-a)F′_(α) where 0.90≤a≤1.8,0≤b≤0.5, 0≤c≤0.05, and 0<α<2; Li_(a)Ni_(1-b-c)Co_(b)B′_(c)O_(2-a)F′₂where 0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05, and 0<α<2;Li_(a)Ni_(1-b-c)Mn_(b)B′_(c)D_(α) where 0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05,and 0<α<2; Li_(a)Ni_(1-b-c)Mn_(b)B′_(c)O_(2-α)F′_(α) where 0.90≤a≤1.8,0≤b≤0.5, 0≤c≤0.05, and 0<α≤2; Li_(a)Ni_(1-b-b)Mn_(b)B′_(c)CO_(2-α)F′₂where 0.90≤a≤1.8, 0≤b≤0.5, 0≤c≤0.05, and 0<α<2; Li_(a)Ni_(b)E_(c)G_(d)O₂where 0.90≤a≤1.8, 0≤b≤0.9, 0≤c≤0.5, and 0.001≤d≤0.1;Li_(a)Ni_(b)Co_(c)Mn_(d)GeO₂ where 0.90≤a≤1.8, 0≤b≤0.9, 0≤c≤0.5,0≤d≤0.5, and 0.001≤e≤0.1; Li_(a)NiG_(b)O₂ where 0.90≤a≤1.8 and0.001≤b≤0.1; Li_(a)CoG_(b)O₂ wherein 0.90≤a≤1.8 and 0.001≤b≤0.1;Li_(a)MnG_(b)O₂ where 0.90≤a≤1.8 and 0.001≤b≤0.1; Li_(a)Mn₂G_(b)O₄ where0.90≤a≤1.8 and 0.001≤b≤0.1; QO₂; QS₂; LiQS₂; V₂O₅; LiV₂O₅; LiI′O₂;LiNiVO₄; Li_((3-f))J₂(PO₄)₃ where 0≤f≤2; Li_((3-f))Fe₂(PO₄)₃ where0≤f≤2; and LiFePO₄.

In the formulae above, A may be selected from nickel (Ni), cobalt (Co),manganese (Mn), and combinations thereof, B′ may be selected fromaluminum (Al), Ni, Co, manganese (Mn), chromium (Cr), iron (Fe),magnesium (Mg), strontium (Sr), vanadium (V), a rare earth element, andcombinations thereof, D may be selected from oxygen (O), fluorine (F),sulfur (S), phosphorus (P), and combinations thereof, E may be selectedfrom Co, Mn, and combinations thereof; F′ may be selected from F, S, P,and combinations thereof; G may be selected from Al, Cr, Mn, Fe, Mg,lanthanum (La), cerium (Ce), Sr, V, and combinations thereof, Q may beselected from titanium (Ti), molybdenum (Mo), Mn, and combinationsthereof, I′ may be selected from Cr, V, Fe, scandium (Sc), yttrium (Y),and combinations thereof, and J may be selected from V, Cr, Mn, Co, Ni,copper (Cu), and combinations thereof.

For example, the cathode active material may be LiCoO₂, LiMn_(x)O_(2x)where x=1 or 2, LiNi_(1-x)Mn_(x)O_(2x) where 0<x<1,LiNi_(1-x-y)Co_(x)Mn_(y)O₂ where 0<1-x-y<0.6, 0≤x≤0.5, and 0≤y≤0.5,LiFePO₄, or the like.

For example, the above-described lithium transition metal oxides ofFormulae 26 to 28 may be used as the cathode active materials.

In addition, the lithium-containing metal oxides described above used asa cathode active material may have a coating layer at their surfaces. Inanother embodiment, a mixture of a lithium-containing metal oxide and alithium-containing metal oxide with a coating layer at a surface thereofmay be used. The coating layer may include a coating element compound,such as an oxide of a coating element, a hydroxide of a coating element,an oxyhydroxide of a coating element, an oxycarbonate of a coatingelement, or a hydroxycarbonate of a coating element. The coating elementcompounds may be amorphous or crystalline. The coating element includedin the coating layer may be selected from Mg, Al, Co, potassium (K),sodium (Na), calcium (Ca), silicon (Si), Ti, V, tin (Sn), germanium(Ge), gallium (Ga), boron (B), arsenic (As), zirconium (Zr), andmixtures thereof. A coating layer may be formed by using the coatingelements in the aforementioned compounds by using a suitable method,(e.g., spray coating, dipping, or the like) that does not adverselyaffect physical properties of the cathode active material.

A suitable conductive material may be used. The conductive material maybe, for example, carbon black, graphite particulates, or the like.

The binder may be a suitable binder used in the art. Examples of thebinder include a vinylidene fluoride/hexafluoropropylene copolymer,polyvinylidene fluoride (PVDF), polyacrylonitrile, polymethylmethacrylate, polytetrafluoroethylene, mixtures thereof, and a styrenebutadiene rubber-based polymer.

The solvent may be, for example, N-methylpyrrolidone, acetone, water, orthe like.

The amounts of the cathode active material, the conductive material, thebinder, and the solvent may be the same amounts as those used in ageneral lithium battery. At least one of the conductive material, thebinder, and the solvent may be omitted according to the use andconstitution of desired lithium batteries.

An anode may be prepared by a suitable fabrication method. For example,an anode active material composition may be prepared by mixing an anodeactive material, a conductive material, a binder, and a solvent. Theanode active material composition may be directly coated onto a metalcurrent collector and dried to obtain an anode plate. In someimplementations, the anode active material composition may be cast ontoa separate support and a film separated from the support may belaminated onto a metal current collector to complete the fabrication ofan anode plate.

As the anode active material, a suitable anode active material forlithium batteries may be used. For example, the anode active materialmay include at least one selected from lithium metal, a metal alloyablewith lithium, a transition metal oxide, a non-transition metal oxide,and a carbonaceous material.

For example, the metal alloyable with lithium may be Si, Sn, Al, Ge,lead (Pb), bismuth (Bi), antimony (Sb), a Si—Y′ alloy (Y′ is an alkalimetal, an alkali earth metal, Group 13 and 14 elements, a transitionmetal, a rare earth element, or a combination thereof, and is not Si), aSn—Y′ alloy (Y′ is an alkali metal, an alkali earth metal, Group 13 and14 elements, a transition metal, a rare earth element, or a combinationthereof, and is not Sn), or the like. The element Y′ may be selectedfrom Mg, Ca, Sr, barium (Ba), radium (Ra), Sc, Y, Ti, Zr, hafnium (Hf),rutherfordium (Rf), V, niobium (Nb), tantalum (Ta), dubnium (db), Cr,Mo, tungsten (W), seaborgium (Sg), technetium (Tc), rhenium (Re),bohrium (Bh), Fe, Pb, ruthenium (Ru), osmium (Os), hassium (Hs), rhodium(Rh), iridium (Ir), palladium (Pd), platinum (Pt), Cu, silver (Ag), gold(Au), zinc (Zn), cadmium (Cd), B, Al, Ga, Sn, indium (In), Ge, P, As,Sb, Bi, S, selenium (Se), tellurium (Te), polonium (Po), andcombinations thereof.

For example, the transition metal oxide may be lithium titanium oxide,vanadium oxide, lithium vanadium oxide, or the like.

For example, the non-transition metal oxide may be SnO₂, SiO_(x) where0<x<2, or the like.

For example, the carbonaceous material may be crystalline carbon,amorphous carbon, or a mixture thereof. Examples of the crystallinecarbon include natural graphite and artificial graphite, each of whichhas an irregular form or is in the form of a plate, a flake, a sphere,or a fiber. Examples of the amorphous carbon include soft carbon(low-temperature calcined carbon), hard carbon, mesophase pitchcarbonized product, and calcined coke.

In the anode active material composition, a conductive material and abinder that are the same as those used in the cathode active materialcomposition may be used.

The amounts of the anode active material, the conductive material, thebinder, and the solvent may be the same amounts as those used in ageneral lithium battery. At least one of the conductive material, thebinder, and the solvent may be omitted according to the use andconstitution of desired lithium batteries.

A suitable separator to be disposed between the cathode and the anodemay be prepared. As the separator, a separator having low resistance tothe transfer of ions in an electrolyte and having a highelectrolyte-retaining ability may be used. Examples of the separator mayinclude glass fiber, polyester, Teflon, polyethylene, polypropylene,polytetrafluoroethylene (PTFE), and combinations thereof, each of whichmay be a non-woven or woven fabric. For example, a windable separatorformed of polyethylene, polypropylene, or the like may be used inlithium ion batteries, and a separator having a high organicelectrolytic solution-retaining ability may be used in lithium ionpolymer batteries. For example, the separator may be manufacturedaccording to the following method.

A polymer resin, a filler, and a solvent may be mixed together toprepare a separator composition. Then, the separator composition may bedirectly coated onto an electrode and dried to form a separator. In animplementation, the separator composition may be cast onto a support anddried, and then a separator film separated from the support may belaminated onto an upper portion of an electrode, thereby completing themanufacture of a separator.

Suitable materials used in binders of electrode plates may in themanufacture of the separator. For example, the polymer resin may be avinylidene fluoride/hexafluoropropylene copolymer, PVDF,polyacrylonitrile, polymethyl methacrylate, a mixture thereof, or thelike.

The organic electrolytic solution as described above may be prepared.

As illustrated in FIG. 7 , a lithium battery 1 may include a cathode 3,an anode 2, and a separator 4. The cathode 3, the anode 2, and theseparator 4 may be wound or folded and then accommodated in a batterycase 5. Subsequently, the organic electrolytic solution may be injectedinto the battery case 5, and the battery case 5 may be sealed with a capassembly 6, thereby completing the manufacture of the lithium battery 1.The battery case 5 may have a cylindrical, rectangular or thin filmshape.

In some implementations, the separator 4 may be disposed between thecathode 3 and the anode 2 to form a battery assembly, a plurality ofbattery assemblies may be stacked in a bi-cell structure and impregnatedwith the organic electrolytic solution, and the resultant may be putinto a pouch and hermetically sealed, thereby completing the manufactureof a lithium battery.

The battery assemblies may be stacked to form a battery pack, and such abattery pack may be used in devices requiring high capacity andhigh-power output. For example, the battery pack may be used in notebookcomputers, smart phones, electric vehicles, or the like.

The lithium battery may have excellent lifespan characteristics and highrate characteristics, and thus, may be used in electric vehicles (EVs).For example, the lithium battery may be used in hybrid vehicles such asa plug-in hybrid electric vehicle (PHEV) or the like. The lithiumbattery may also be used in fields requiring the storage of a largeamount of power. For example, the lithium battery may be used inelectric bikes, motor-driven tools, or the like.

The following Examples and Comparative Examples are provided in order tohighlight characteristics of one or more embodiments, but it will beunderstood that the Examples and Comparative Examples are not to beconstrued as limiting the scope of the embodiments, nor are theComparative Examples to be construed as being outside the scope of theembodiments. Further, it will be understood that the embodiments are notlimited to the particular details described in the Examples andComparative Examples.

Synthesis of Additive Preparation Example 1: Synthesis of Compound ofFormula 3

The compound of Formula 3 may be prepared according to Reaction Scheme 1below:

Synthesis of Compound A

68.0 g (0.499 mol) of pentaerythritol and 100 g of molecular sieve (Type4A) were added to a mixed solvent of tetrahydrofuran (THF) anddichloromethane (DCM, CH₂Cl₂) in a volume ratio of 1:1 and the resultingsolution was refluxed for 20 minutes. Subsequently, 110 ml (2.8 equiv.,1.40 mol) of thionyl chloride (SOCl₂) was added to the resultant and theresultant solution was refluxed for 8 hours until the pentaerythritolwas completely consumed by reaction, to obtain a light yellow solution.The obtained light yellow solution was filtered and concentrated toobtain a residue including a light yellow solid. Thereafter, 1 L of asaturated sodium hydrogen carbonate (NaHCO₃) solution was directly addedto the residue at a rate at which effervescence was minimized, to obtaina suspension. The suspension was vigorously stirred for 20 minutes.Thereafter, the suspension was filtered and the obtained solid was addedto 1 L of purified water to prepare a mixture. Then, the mixture wasvigorously stirred for 20 minutes, subjected to suction filtration, anddried in air to obtain 104.61 g (0.458 mol) of Compound A (yield: 92%).

¹H-NMR and ¹³C-NMR data of Compound A were same as those in documents.

Synthesis of Compound B

As shown in Reaction Scheme 1 above, Compound B represented by Formula 6below was synthesized from Compound A according to a method disclosed inCanadian Journal of Chemistry, 79, 2001, page 1042.

The synthesized compound was recrystallized in a mixed solvent of1,2-dichloroethane and acetonitrile in a volume ratio of 2:1, which wasthen used in the preparation of an electrolytic solution.

Preparation of Organic Electrolytic Solution Example 1: SEI-1316 1.0 wt%

0.90 M LiPF₆ as a lithium salt and 1 wt % of the compound of Formula 6were added to a mixed solvent of ethylene carbonate (EC), ethyl methylcarbonate (EMC), and diethyl carbonate (DEC) in a volume ratio of 3:5:2to prepare an organic electrolytic solution.

Example 2: SEI-1316 1.0 wt %+VC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that 1 wt % of the compound of Formula 6 and 0.5 wt %of vinylene carbonate (VC) were used as additives.

Example 3: SEI-1316 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 0.5 wt %.

Example 4: SEI-1316 0.2 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 0.2 wt %.

Example 5: SEI-1316 0.3 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 0.3 wt %.

Example 6: SEI-1316 0.7 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 0.7 wt %.

Example 7: SEI-1316 1.5 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 1.5 wt %.

Example 8: SEI-1316 2 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 2 wt %.

Example 9: SEI-1316 3 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 3 wt %.

Example 9a: SEI-1316 4 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 4 wt %.

Example 10: SEI-1316 5 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the amount of the compound of Formula 6 used asan additive was changed to 5 wt %.

Comparative Example 1: SEI-1316 0 wt %

An organic electrolytic solution was prepared in the same manner as inExample 1, except that the compound of Formula 6 used as an additive wasnot used.

Preparation of Organic Electrolytic Solution Example K1: SEI-1316 1.0 wt%+OA1300 1.0 wt %+VC 1.5 wt %+VEC 0.5 wt %

1.15 M LiPF₆ as a lithium salt and 1.0 wt % of the compound of Formula6, 1.0 wt % of a compound of Formula K4 below, 1.5 wt % of vinylenecarbonate (VC), and 0.5 wt % of vinyl ethyl carbonate (VEC) as additiveswere added to a mixed solvent of ethylene carbonate (EC), ethyl methylcarbonate (EMC), and dimethyl carbonate (DMC) in a volume ratio of 2:4:4to prepare an organic electrolytic solution.

Example K2: SEI-1316 1.0 wt %+OA1300 0.25 wt %+VC 1.5 wt %+VEC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the amount of the compound ofFormula K4 was changed to 0.25 wt %.

Example K3: SEI-1316 1.0 wt %+OA1300 0.5 wt %+VC 1.5 wt %+VEC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the amount of the compound ofFormula K4 was changed to 0.5 wt %.

Example K4: SEI-1316 1.0 wt %+OA1300 3.0 wt %+VC 1.5 wt %+VEC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the amount of the compound ofFormula K4 was changed to 3 wt %.

Example K5: SEI-1316 1.0 wt %+OA1301 1.0 wt %+VC 1.5 wt %+VEC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that a compound of Formula K5 below wasused instead of the compound of Formula K4.

Example K6: SEI-1316 1.0 wt %+OA1301 0.5 wt %+VC 1.5 wt %+VEC 0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula K5 was usedinstead of the compound of Formula K4, and the amount of the compound ofFormula K5 was changed to 0.5 wt %.

Comparative Example K1: SEI-1316 1.0 wt %+OA1301 0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula K4 was notused.

Comparative Example K2: SEI-1316 2.0 wt %+OA1301 0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the amount of the compound ofFormula 6 was changed to 2.0 wt %, and the compound of Formula K4 wasnot used.

Comparative Example K3: SEI-1316 0 wt %+OA1301 1.0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula 6 was notused.

Comparative Example K4: SEI-1316 0 wt %+OA1301 0.5 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula 6 was notused, and the amount of the compound of Formula K4 was changed to 0.5 wt%.

Comparative Example K5: SEI-1316 0 wt %+OA1301 3 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula 6 was notused, and the amount of the compound of Formula K4 was changed to 3.0 wt%.

Comparative Example K6: SEI-1316 1.0 wt %+TEPi 1.0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that a compound of Formula K15 below wasused instead of the compound of Formula K4.

Comparative Example K7 SEI-1316 3.0 wt %+TEPi 0.5 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula K15 was usedinstead of the compound of Formula K4, and the amount of the compound ofFormula K15 was changed to 0.5 wt %.

Comparative Example K8: SEI-1316 0 wt %+TEPa 1.0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that a compound of Formula K16 below wasused instead of the compound of Formula K4.

Comparative Example K9: SEI-1316 0 wt %+TEPa 0.5 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula K16 was usedinstead of the compound of Formula K4, and the amount of the compound ofFormula K16 was changed to 0.5 wt %.

Comparative Example K10: SEI-1316 0 wt %+TFEP 1.0 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that a compound of Formula K17 below wasused instead of the compound of Formula K4.

Comparative Example K11. SEI-1316 0 wt %+TFEP 0.5 wt %+VC 1.5 wt %+VEC0.5 wt %

An organic electrolytic solution was prepared in the same manner as inPreparation Example K1, except that the compound of Formula K17 was usedinstead of the compound of Formula K4, and the amount of the compound ofFormula K17 was changed to 0.5 wt %.

Manufacture of Lithium Battery (Examples 1-1 to 3-1 and ComparativeExample 1-1) Example 1-1

Manufacture of Anode

98 wt % of artificial graphite (BSG-L manufactured by Tianjin BTR NewEnergy Technology Co., Ltd.), 1.0 wt % of styrene-butadiene rubber (SBR)(manufactured by Zeon) as a binder, and 1.0 wt % of carboxymethylcellulose (CMC) (manufactured by NIPPON A&L) were mixed together, themixture was added to distilled water, and the resulting solution wasstirred using a mechanical stirrer for 60 minutes to prepare an anodeactive material slurry. The anode active material slurry was applied,using a doctor blade, onto a copper (Cu) current collector having athickness of 10 μm to a thickness of about 60 μm, and the currentcollector was dried in a hot-air dryer at 100° C. for 0.5 hours,followed by further drying under conditions: in vacuum at 120° C. for 4hours, and roll-pressed, thereby completing the manufacture of an anodeplate.

Manufacture of Cathode

97.45 wt % of LiNi_(1/3)Co_(1/3)Mn_(1/3)O₂, 0.5 wt % of powder-typeartificial graphite (SFG6 manufactured by Timcal) as a conductivematerial, 0.7 wt % of carbon black (Ketjen black manufactured by ECP),0.25 wt % of modified acrylonitrile rubber (BM-720H manufactured by ZeonCorporation), 0.9 wt % of polyvinylidene fluoride (PVdF, S6020manufactured by Solvay), and 0.2 wt % of PVdF (S5130 manufactured bySolvay) were mixed together, the mixture was added toN-methyl-2-pyrrolidone as a solvent, and the resulting solution wasstirred using a mechanical stirrer for 30 minutes to prepare a cathodeactive material slurry. The cathode active material slurry was applied,using a doctor blade, onto an aluminum (Al) current collector having athickness of 20 μm to a thickness of about 60 μm, and the currentcollector was dried in a hot-air dryer at 100° C. for 0.5 hours,followed by further drying under conditions: in vacuum at 120° C. for 4hours, and roll-pressed, thereby completing the manufacture of a cathodeplate.

A polyethylene separator having a thickness of 14 μm (manufactured by SKInnovation), a cathode side of which was coated with ceramic, and theorganic electrolytic solution prepared according to Example 1 were usedto complete the manufacture of a lithium battery.

Examples 2-1 to 3-1

Lithium batteries were manufactured in the same manner as in Example1-1, except that the organic electrolytic solutions prepared accordingto Examples 2 and 3, respectively were used instead of the organicelectrolytic solution of Example 1.

Comparative Example 1-1

A lithium battery was manufactured in the same manner as in Example 1-1,except that the organic electrolytic solution prepared according toComparative Example 1 was used instead of the organic electrolyticsolution of Example 1.

Evaluation Example 1: Evaluation of Charge and Discharge Characteristicsat 4.25 V and Room Temperature (25° C.)

The lithium batteries manufactured according to Examples 1-1 to 3-1 andComparative Example 1-1 were each charged at a constant current of 0.1 Crate at 25° C. until the voltage reached 4.25 V (vs. Li) and then, whilemaintaining a constant voltage of 4.25 V, the charging process was cutoff at a current of 0.05 C rate. Subsequently, each lithium battery wasdischarged with a constant current of 0.1 C rate until the voltagereached 2.8 V (vs. Li) (formation operation, 1^(st) cycle).

Each lithium battery after the 1^(st) cycle of the formation operationwas charged at a constant current of 0.2 C rate at 25° C. until thevoltage reached 4.25 V (vs. Li) and then, while maintaining a constantvoltage of 4.25 V, the charging process was cut off at a current of 0.05C rate. Subsequently, each lithium battery was discharged at a constantcurrent of 0.2 C rate until the voltage reached 2.8 V (vs. Li)(formation operation, 2^(nd) cycle).

Each lithium battery after the 2^(nd) cycle of the formation operationwas charged at a constant current of 1.0 C rate at 25° C. until thevoltage reached 4.25 V (vs. Li) and then, while maintaining a constantvoltage of 4.25 V, the charging process was cut off at a current of 0.05C rate. Subsequently, each lithium battery was discharged at a constantcurrent of 1.0 C rate until the voltage reached 2.75 V (vs. Li), andthis cycle of charging and discharging was repeated 380 times.

In all the cycles of charging and discharging, there was a rest periodof 10 minutes at the end of each cycle of charging/discharging.

A part of the charging and discharging experiment results is shown inTable 1 below and FIGS. 1 and 2 . A capacity retention ratio at the380^(th) cycle is defined using Equation 1 below:

Capacity retention ratio=[discharge capacity at 380^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation 1

TABLE 1 Discharge capacity Capacity retention at 380^(th) ratio at380^(th) cycle [mAh/g] cycle [%] Example 1-1 202 75 Example 2-1 228 82Comparative 173 63 Example 1-1

As shown in Table 1 and FIGS. 1 and 2 , the lithium batteries ofExamples 1-1 and 2-1 including the additives according to embodiments ofthe present disclosure exhibited, at room temperature, significantlyenhanced discharge capacities and lifespan characteristics, as comparedto the lithium battery of Comparative Example 1-1 not including such anadditive.

Evaluation Example 2: Evaluation of Charge and Discharge Characteristicsat 4.25 V and High Temperature (45° C.)

Charge and discharge characteristics of the lithium batteries ofExamples 1-1 to 3-1 and Comparative Example 1-1 were evaluated using thesame method as that used in Evaluation Example 1, except that thecharging and discharging temperature was changed to 45° C. Meanwhile,the number of charging and discharging cycles was changed to 200 cycles.

A part of the charging and discharging experiment results is shown inTable 2 below and FIGS. 3 and 4 . A capacity retention ratio at the200^(th) cycle is defined using Equation 2 below:

Capacity retention ratio=[discharge capacity at 200^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation 2

TABLE 2 Discharge capacity Capacity retention at 200^(th) ratio at200^(th) cycle [mAh/g] cycle [%] Example 1-1 249 83 Example 2-1 255 84Comparative 235 79 Example 1-1

As shown in Table 2 and FIGS. 3 and 4 , the lithium batteries ofExamples 1-1 and 2-1 including the additives according to embodiments ofthe present disclosure exhibited, at a high temperature, significantlyenhanced discharge capacities and lifespan characteristics, as comparedto the lithium battery of Comparative Example 1-1 not including such anadditive.

Evaluation Example 3: Evaluation of Charge and Discharge Characteristicsat 4.30 V and Room Temperature (25° C.)

The lithium batteries of Example 1-1 and Comparative Example 1-1 wereeach charged at a constant current of 0.1 C rate at 25° C. until thevoltage reached 4.30 V (vs. Li) and then, while maintaining a constantvoltage of 4.30 V, the charging process was cut off at a current of 0.05C rate. Subsequently, each lithium battery was discharged at a constantcurrent of 0.1 C rate until the voltage reached 2.8 V (vs. Li)(formation operation, 1^(st) cycle).

Each lithium battery after the 1^(st) cycle of the formation operationwas charged at a constant current of 0.2 C rate at 25° C. until thevoltage reached 4.30 V (vs. Li) and then, while maintaining a constantvoltage of 4.30 V, the charging process was cut off at a current of 0.05C rate. Subsequently, each lithium battery was discharged at a constantcurrent of 0.2 C rate until the voltage reached 2.8 V (vs. Li)(formation operation, 2^(nd) cycle).

Each lithium battery after the 2^(nd) cycle of the formation operationwas charged at a constant current of 0.5 C rate at 25° C. until thevoltage reached 4.30 V (vs. Li) and then, while maintaining a constantvoltage of 4.30 V, the charging process was cut off at a current of 0.05C rate. Subsequently, each lithium battery was discharged at a constantcurrent of 1.0 C rate until the voltage reached 2.75 V (vs. Li), andthis cycle of charging and discharging was repeated 250 times.

In all the cycles of charging and discharging, there was a rest periodof 10 minutes at the end of each cycle of charging/discharging.

A part of the charging and discharging experiment results is shown inTable 3 below and FIG. 5 . A capacity retention ratio at 250^(th) cycleis defined using Equation 3 below:

Capacity retention ratio=[discharge capacity at 250^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation 3

TABLE 3 Discharge capacity Capacity retention at 250^(th) ratio at250^(th) cycle [mAh/g] cycle [%] Example 1-1 171 84 Comparative 154 77Example 1-1

As shown in Table 3 and FIG. 5 , the lithium battery of Example 1-1including the additive according to an embodiment of the presentdisclosure exhibited, at room temperature, significantly enhanceddischarge capacity and lifespan characteristics, as compared to thelithium battery of Comparative Example 1-1 not including such anadditive.

Evaluation Example 4: Evaluation of Charge and Discharge Characteristicsat 4.30 V and High Temperature (45° C.)

Charge and discharge characteristics of the lithium batteries of Example1-1 and Comparative Example 1-1 were evaluated using the same method asthat used in Evaluation Example 3, except that the charging anddischarging temperature was changed to 45° C. Also, the number ofcharging and discharging cycles was changed to 200^(th) cycles.

A part of the charging and discharging experiment results is shown inTable 4 below and FIG. 6 . A capacity retention ratio at the 200^(th)cycle is defined using Equation 4 below:

Capacity retention ratio=[discharge capacity at 200^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation 4

TABLE 4 Discharge capacity Capacity retention at 200^(th) ratio at200^(th) cycle [mAh/g] cycle [%] Example 1-1 189 90 Comparative 174 84Example 1-1

As shown in Table 4 and FIG. 6 , the lithium battery of Example 1-1including the additive according to an embodiment of the presentdisclosure exhibited, at a high temperature, significantly enhanceddischarge capacity and lifespan characteristics, as compared to thelithium battery of Comparative Example 1-1 not including such anadditive.

Evaluation Example 5: High-Temperature (60° C.) Stability Evaluation

The lithium batteries of Examples 1-1 to 3-1 and Comparative Example 1-1were subjected to the 1^(st) cycle of charging and discharging asfollows. Each lithium battery was charged at a constant current of 0.5 Crate at 25° C. until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.5 C rate until the voltage reached 2.8 V.

Each lithium battery was subjected to the 2^(nd) cycle of charging anddischarging as follows. Each lithium battery was charged at a constantcurrent of 0.5 C rate until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.2 C rate until the voltage reached 2.8 V.

Each lithium battery was subjected to the 3^(rd) cycle of charging anddischarging as follows. Each lithium battery was charged at a constantcurrent of 0.5 C rate until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.2 C rate until the voltage reached 2.80 V. Adischarge capacity at the 3^(rd) cycle was regarded as a standardcapacity.

Each lithium battery was subjected to the 4^(th) cycle of charging anddischarging as follows. Each lithium battery was charged at 0.5 C rateuntil the voltage reached 4.30 V and then, while maintaining a constantvoltage of 4.30 V, each lithium battery was charged until the currentreached 0.05 C, the charged battery was stored in an oven at 60° C. for10 days and 30 days, and then the battery was taken out of the oven andthen discharged at 0.1 C rate until the voltage reached 2.80 V.

A part of the charging and discharging evaluation results is shown inTable 5 below. A capacity retention ratio after the high-temperaturestorage is defined using Equation 5 below:

Capacity retention ratio after high-temperature storage [%]=[dischargecapacity at high temperature at 4^(th) cycle/standard capacity]×100(herein, the standard capacity is a discharge capacity at 3^(rd)cycle)  Equation 5

TABLE 5 Capacity retention Capacity retention ratio after 10-day ratioafter 30-day storage [%] storage [%] Example 3-1 91 87 Comparative 90 86Example 1-1

As shown in Table 5, the lithium battery of Example 3-1 including theorganic electrolytic solution according to an embodiment of the presentdisclosure exhibited significantly enhanced high-temperature stability,as compared to the lithium battery of Comparative Example 1-1 notincluding the organic electrolytic solution of the present invention.

Evaluation Example 6: Direct Current Resistance (DC-IR) Evaluation afterHigh-Temperature (60° C.) Storage

DC-IR of each of the lithium batteries of Examples 1-1 to 3-1 andComparative Example 1-1, before being left sit in a 60° C. oven, after10-day storage in an oven at 60° C., and after 30-day storage in an ovenat 60° C., was measured at room temperature (25° C.) using the followingmethod.

Each lithium battery was subjected to 1^(st) cycle of charging anddischarging as follows. Each lithium battery was charged at a current of0.5 C until the voltage reached 50% SOC (state of charge), the chargingprocess was cut off at 0.02 C, and then each lithium battery rested for10 minutes. Subsequently, each lithium battery was subjected to thefollowing processes: discharging at a constant current of 0.5 C for 30seconds, followed by resting for 30 seconds, and charging at a constantcurrent of 0.5 C for 30 seconds, followed by resting for 10 minutes;discharging at a constant current of 1.0 C for 30 minutes, followed byresting for 30 seconds, and charging at a constant current of 0.5 C for1 minute, followed by resting for 10 minutes; discharging at a constantcurrent of 2.0 C for 30 seconds, followed by resting for 30 seconds, andcharging at a constant current of 0.5 C for 2 minutes, followed byresting for 10 minutes; discharging at a constant current of 3.0 C for30 seconds, followed by resting for 30 seconds, and charging at aconstant current of 0.5 C for 2 minutes, followed by resting for 10minutes.

An average voltage drop value for 30 seconds at each C-rate is a directcurrent voltage value.

A part of direct current resistance increases calculated from measuredinitial direct current resistances and direct current resistances afterhigh-temperature storage is shown in Table 6 below. A direct currentresistance increase is represented by Equation 6 below:

Direct current resistance increase [%]=[direct current resistance afterhigh-temperature storage/initial direct currentresistance]×100  Equation 6

TABLE 6 Direct current resistance Direct current resistance increaseafter increase after 10-day storage [%] 30-day storage [%] Example 3-1113 125 Comparative 122 137 Example 1-1

As shown in Table 6, the lithium battery of Example 3-1 including theorganic electrolytic solution according to an embodiment of the presentdisclosure exhibited a decrease in direct current resistance increaseafter high-temperature storage, as compared to the lithium battery ofComparative Example 1-1 not including the organic electrolytic solution.

Manufacture of Lithium Battery

Example A1: NCM, Ni60+SEI-1316 0.5 wt %

Manufacture of Anode

98 wt % of artificial graphite (BSG-L manufactured by Tianjin BTR NewEnergy Technology Co., Ltd.), 1.0 wt % of styrene-butadiene rubber (SBR)(manufactured by Zeon) as a binder, and 1.0 wt % of carboxymethylcellulose (CMC) (manufactured by NIPPON A&L) were mixed together, themixture was added to distilled water, and the resulting solution wasstirred using a mechanical stirrer for 60 minutes to prepare an anodeactive material slurry. The anode active material slurry was applied,using a doctor blade, onto a Cu current collector having a thickness of10 μm to a thickness of about 60 μm, and the current collector was driedin a hot-air dryer at 100° C. for 0.5 hours, followed by further dryingin vacuum at 120° C. for 4 hours, and roll-pressed, thereby completingthe manufacture of an anode plate.

Manufacture of Cathode

97.45 wt % of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, 0.5 wt % ofpowder-type artificial graphite (SFG6 manufactured by Timcal) as aconductive material, 0.7 wt % of carbon black (Ketjen black manufacturedby ECP), 0.25 wt % of modified acrylonitrile rubber (BM-720Hmanufactured by Zeon Corporation), 0.9 wt % of polyvinylidene fluoride(PVdF) (S6020 manufactured by Solvay), and 0.2 wt % of PVdF (S5130manufactured by Solvay) were mixed together, the mixture was added toN-methyl-2-pyrrolidone as a solvent, and the resulting solution wasstirred using a mechanical stirrer for 30 minutes to prepare a cathodeactive material slurry. The cathode active material slurry was applied,using a doctor blade, onto an aluminum (Al) current collector having athickness of 20 μm to a thickness of about 60 μm, and the currentcollector was dried in a hot-air dryer at 100° C. for 0.5 hours,followed by further drying in vacuum at 120° C. for 4 hours, androll-pressed, thereby completing the manufacture of a cathode plate.

A polyethylene separator having a thickness of 14 μm, a cathode side ofwhich was coated with ceramic, and the organic electrolytic solutionprepared according to Example 3 were used to complete the manufacture ofa lithium battery.

Example A2: NCM, Ni60+SEI-1316 0.7 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 6 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Example A3: NCM, Ni60+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 1 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Example A4: NCM, Ni60+SEI-1316 1.5 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 7 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Example A5: NCM, Ni60+SEI-1316 3 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 9 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Example A6: NCM, Ni88+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Mn_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 1 was used as anelectrolytic solution.

Example A7: NCA, Ni88+SEI-1316 0.5 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂.

Example A8: NCA, Ni88+SEI-1316 0.7 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 6 was used as anelectrolytic solution.

Example A9: NCA, Ni88+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 1 was used as anelectrolytic solution.

Example A10: NCA, Ni88+SEI-1316 3 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution prepared according to Example 9 wasused as an electrolytic solution.

Example A11: NCA, Ni91+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.91)Co_(0.05)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 1 was used as anelectrolytic solution.

Reference Example A1: Ni55+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.55)Co_(0.25)Mn_(0.20)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 1 was used as anelectrolytic solution.

Reference Example A2: NCM, Ni60+SEI-1316 0.2 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 4 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Reference Example A3: NCM, Ni60+SEI-1316 5 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toExample 10 was used as an electrolytic solution instead of the organicelectrolytic solution of Example 3.

Reference Example A4: NCA, Ni88+SEI-1316 0.2 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution prepared according to Example 4 wasused as an electrolytic solution instead of the organic electrolyticsolution of Example 3.

Reference Example A5: NCA, Ni88+SEI-1316 5 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that Li_(1.02)Ni_(0.88)Co_(0.08)Al_(0.04)O₂ was used as a cathodeactive material instead of Li_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, andthe organic electrolytic solution of Example 10 was used as anelectrolytic solution instead of the organic electrolytic solution ofExample 3.

Comparative Example A1: Ni60+SEI-1316 0 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that the organic electrolytic solution prepared according toComparative Example 1 was used instead of the organic electrolyticsolution of Example 3.

Comparative Example A2: LCO, Ni00+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that LiCoO₂ was used as a cathode active material instead ofLi_(1.02)Ni_(0.60)Co_(0.20)Mn_(0.20)O₂, and the organic electrolyticsolution of Example 1 was used as an electrolytic solution.

Comparative Example A3: NCM+LMO+SEI-1316 1 wt %

A lithium battery was manufactured in the same manner as in Example A1,except that a mixture of LiNi_(1/3)Co_(1/3)Mn_(1/3)O₂ and LiMn₂O₄ in aweight ratio of 1:1 was used as a cathode active material instead ofLi_(1.02)Ni_(0.85)Co_(0.10)Mn_(0.05)O₂, and the organic electrolyticsolution of Example 1 was used as an electrolytic solution.

Evaluation Example A1: Evaluation of Charge/Discharge Characteristics at4.25 V and Room Temperature (25° C.)

Charge/discharge characteristics of the lithium batteries manufacturedaccording to Examples A1 to A11, Reference Examples A1 to A5, andComparative Examples A1 to A3 were evaluated using the same method asthat used in Evaluation Example 1.

A part of the charging and discharging experiment results is shown inTable A1 below. A capacity retention ratio at the 380^(th) cycle isdefined using Equation 1 below:

Capacity retention ratio=[discharge capacity at 380^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation 1

TABLE A1 Capacity retention ratio at 380^(th) cycle [%] Example A1 (NCM,Ni60 + SEI-1316 0.5 wt %) 94 Example A2 (NCM, Ni60 + SEI-1316 0.7 wt %)94 Example A3 (NCM, Ni60 + SEI-1316 1 wt %) 95 Example A4 (NCM, Ni60 +SEI-1316 1.5 wt %) 95 Example A5 NCM, (Ni60 + SEI-1316 3 wt %) 93Example A6 (NCM, Ni88 + SEI-1316 1 wt %) 94 Example A7 (NCA, Ni88 +SEI-1316 0.5 wt %) 93 Example A8 (NCA, Ni88 + SEI-1316 0.7 wt %) 94Example A9 (NCA, Ni88 + SEI-1316 1 wt %) 94 Example A10 (NCA, Ni88 +SEI-1316 3 wt %) 92 Example A11 (NCA, Ni91 + SEI-1316 1 wt %) 93Reference Example A1 (NCM, Ni55 + SEI-1316 1 wt %) 90 Reference ExampleA2 (NCM, Ni60 + SEI-1316 0.2 wt %) 92 Reference Example A3 (NCM, Ni60 +SEI-1316 5 wt %) wt %) 93 Reference Example A4 (NCA, Ni88 + SEI-1316 0.2wt %) 93 Reference Example A5 (NCA, Ni88 + SEI-1316 5 wt %) 91Comparative Example A1 (NCM, Ni60 + SEI-1316 0 wt %) 85 ComparativeExample A2 (LCO, Ni00 + SEI-1316 1 wt %) 83 Comparative Example A3(NCM + LMO + SEI-1316 1 wt %) 85

As shown in Table A1, the lithium batteries of Examples A1 to A11including the additives and the cathode active materials having highnickel content of the present disclosure exhibited significantlyenhanced lifespan characteristics at room temperature, as compared tothe lithium batteries of Reference Examples A1 and A2 and ComparativeExample A1, including a cathode active material having low nickelcontent or not including an additive.

In addition, the lithium batteries of Examples A1 to A11 each includinga certain amount of additive exhibited more enhanced lifespancharacteristics at room temperature than those of the lithium batteriesof Reference Examples A4 to A7 each including an additive in an amountoutside the certain range.

Evaluation Example A2: Direct Current-Internal Resistance (DC-IR)Evaluation after High-Temperature (60° C.) Storage

DC-IRs after high-temperature storage of the lithium batteries ofExamples A1 to A11, Reference Examples A1 to A7, and Comparative ExampleA1 were measured using the same method as that used in EvaluationExample 6.

A part of DC-IR increases, which were obtained by calculation using themeasured initial DC-IRs and the measured DC-IRs after high-temperaturestorage, is shown in Table A2 below. A DC-IR increase is represented byEquation 6 below:

Direct current internal resistance increase [%]=[direct current internalresistance after high-temperature storage/initial direct currentinternal resistance]×100  Equation 6

TABLE A2 Direct current internal resistance increase after 30-daystorage [%] Example A1 (NCM, Ni60 + SEI-1316 0.5 wt %) 128.4 Example A2(NCM, Ni60 + SEI-1316 0.7 wt %) 127.0 Example A3 (NCM, Ni60 + SEI-1316 1wt %) 125.3 Example A4 (NCM, Ni60 + SEI-1316 1.5 wt %) 124.8 Example A5NCM, (Ni60 + SEI-1316 3 wt %) 126.2 Example A6 (NCM, Ni88 + SEI-1316 1wt %) 127.6 Example A7 (NCA, Ni88 + SEI-1316 0.5 wt %) 128.1 Example A8(NCA, Ni88 + SEI-1316 0.7 wt %) 128.1 Example A9 (NCA, Ni88 + SEI-1316 1wt %) 126.4 Example A10 (NCA, Ni88 + SEI-1316 3 wt %) 128.3 Example A11(NCA, Ni91 + SEI-1316 1 wt %) 126.1 Reference Example A1 (NCM, Ni55 +SEI-1316 1 wt %) 137.1 Reference Example A2 (NCM, Ni60 + SEI-1316 0.2 wt%) 132.3 Reference Example A3 (NCM, Ni60 + SEI-1316 5 wt %) 130.0Reference Example A4 (NCA, Ni88 + SEI-1316 0.2 wt %) 130.0 ReferenceExample A5 (NCA, Ni88 + SEI-1316 5 wt %) 132.7 Comparative Example A1(NCM, Ni60 + SEI-1316 0 wt %) 135.2 Comparative Example A2 (LCO, Ni00 +SEI-1316 1 wt %) 141.3 Comparative Example A3 (NCM + LMO + SEI-1316 1 wt%) 139.5

As shown in Table A2, the lithium batteries of Examples A1 to A11including the additives and the cathode active materials having highnickel content of the present disclosure exhibited a lower DC-IRincrease than that of each of the lithium batteries of ComparativeExamples A1 to A3, which included a cathode active material having lownickel content and did not include an additive.

In addition, the lithium batteries of Examples A1 to A11 each includinga certain amount of additive exhibited a lower DC-IR increase than thatof each of the lithium batteries of Reference Examples A1 to A5including an additive in an amount outside the certain range.

Manufacture of Lithium Battery

Example K7: SEI-1316 1.0 wt %+OA1300 1.0 wt %

Manufacture of Anode

98 wt % of artificial graphite (BSG-L manufactured by Tianjin BTR NewEnergy Technology Co., Ltd.), 1.0 wt % of styrene-butadiene rubber (SBR)(manufactured by Zeon) as a binder, and 1.0 wt % of carboxymethylcellulose (CMC) (manufactured by NIPPON A&L) were mixed together, themixture was added to distilled water, and the resulting solution wasstirred using a mechanical stirrer for 60 minutes to prepare an anodeactive material slurry. The anode active material slurry was applied,using a doctor blade, onto a copper (Cu) current collector having athickness of 10 μm to a thickness of about 60 μm, and the currentcollector was dried in a hot-air dryer at 100° C. for 0.5 hours,followed by further drying under conditions: in vacuum at 120° C. for 4hours, and roll-pressed, thereby completing the manufacture of an anodeplate.

Manufacture of Cathode

97.45 wt % of LiNi_(1/3)Co_(1/3)Mn_(1/3)O₂, 0.5 wt % of powder-typeartificial graphite (SFG6 manufactured by Timcal) as a conductivematerial, 0.7 wt % of carbon black (Ketjen black manufactured by ECP),0.25 wt % of modified acrylonitrile rubber (BM-720H manufactured by ZeonCorporation), 0.9 wt % of polyvinylidene fluoride (PVdF) (S6020manufactured by Solvay), and 0.2 wt % of PVdF (S5130 manufactured bySolvay) were mixed together, the mixture was added toN-methyl-2-pyrrolidone as a solvent, and the resulting solution wasstirred using a mechanical stirrer for 30 minutes to prepare a cathodeactive material slurry. The cathode active material slurry was applied,using a doctor blade, onto an aluminum (Al) current collector having athickness of 20 μm to a thickness of about 60 μm, and the currentcollector was dried in a hot-air dryer at 100° C. for 0.5 hours,followed by further drying under conditions: in vacuum at 120° C. for 4hours, and roll-pressed, thereby completing the manufacture of a cathodeplate.

A polyethylene separator having a thickness of 14 μm, a cathode side ofwhich was coated with ceramic, and the organic electrolytic solutionprepared according to Example K1 were used to complete the manufactureof a lithium battery.

Examples K8 to K12

Lithium batteries were manufactured in the same manner as in Example K7,except that the organic electrolytic solutions prepared according toExamples K2 to K6, respectively were used instead of the organicelectrolytic solution prepared according to Example K1.

Comparative Examples K12 to K22

Lithium batteries were manufactured in the same manner as in Example K7,except that the organic electrolytic solutions prepared according toComparative Examples K1 to K11, respectively were used instead of theorganic electrolytic solution prepared according to Example K1.

Evaluation Example K1: Direct Current Internal Resistance (DC-IR)Evaluation (I) after Evaluation of Lifespan Characteristics at 4.25 Vand High Temperature (45° C.) and High-Temperature Lifespan Evaluation

High-temperature charge/discharge characteristics of the lithiumbatteries manufactured according to Examples K7 to K12 and ComparativeExamples K12 to K16 were evaluated using the same method as that used inEvaluation Example 1, except that the charging/discharging temperaturewas changed to 45° C., and the charging voltage was changed to 4.25 V,and the cycles of charging and discharging were changed to 900 cycles. Apart of the charging and discharging experiment results is shown inTable K1 below. A capacity retention ratio at the 900^(th) cycle isdefined using Equation K1 below:

Capacity retention ratio=[discharge capacity at 900^(th) cycle/dischargecapacity at 1^(st) cycle]×100  Equation K1

DC-IRs of the lithium batteries manufactured according to Examples K7 toK12 and Comparative Examples K12 to K16 and the lithium batteriesthereof after the evaluation of high-temperature lifespancharacteristics was completed were measured using the following method.

In the 1^(st) cycle, each lithium battery was charged at a current of0.5 C until the voltage reached 50% SOC (state of charge), followed byresting for 10 minutes, and was discharged at a constant current of 1.0C for 30 minutes.

The current applied during discharging for 30 minutes and the voltageafter discharging were measured, and DC-IR was calculated therefrom.

Initial direct current resistances of the lithium batteries manufacturedaccording to Examples K7 to K12 and Comparative Examples K12 to K16 weremeasured.

DC-IRs of the lithium batteries after the lifespan characteristics athigh temperature were evaluated were measured after high-temperaturelifespan evaluation.

A part of direct current resistance increases calculated from themeasured initial direct current resistances and the direct currentresistances after high-temperature lifespan evaluation is shown in TableK1 below. A direct current resistance increase is represented byEquation J2 below:

Direct current resistance increase [%]=[direct current resistance afterhigh-temperature lifespan evaluation/initial direct currentresistance]×100  Equation J2

TABLE K1 Direct current internal resistance Capacity increase retentionafter high- ratio at temperature 900^(th) lifespan cycle evaluation [%][%] Example K7 78.1 179.9 (SEI-1316 1.0 wt % + OA1300 1.0 wt %) ExampleK8 77.7 172.1 (SEI-1316 1.0 wt % + OA1300 0.25 wt %) Example K9 78.0173.7 (SEI-1316 1.0 wt % + OA1300 0.5 wt %) Example K10 77.2 183.7(SEI-1316 1.0 wt % + OA1300 3.0 wt %) Example K11 77.5 177.5 (SEI-13161.0 wt % + OA1301 1.0 wt %) Example K12 77.3 178.0 (SEI-1316 1.0 wt % +OA1301 0.5 wt %) Comparative Example K12 73.2 188.1 (SEI-1316 1.0 wt % +OA1300 0 wt %) Comparative Example K13 72.9 189.5 (SEI-1316 2.0 wt % +OA1300 0 wt %) Comparative Example K14 72.6 189.3 (SEI-1316 0 wt % +OA1300 1.0 wt %) Comparative Example K15 72.5 190.4 (SEI-1316 0 wt % +OA1300 0.5 wt %) Comparative Example K16 72.1 189.9 (SEI-1316 0 wt % +OA1300 3.0 wt %)

As shown in Table K1, the lithium batteries of Examples K7 to K12including both of the two additives of the present disclosure exhibitedimproved high-temperature lifespan characteristics, as compared to thelithium batteries of Comparative Examples K12 to K16 including anadditive alone.

In addition, the lithium batteries of Examples K7 to K12 including bothof the two additives of the present disclosure exhibited lower directcurrent internal resistance increases, as compared to the lithiumbatteries of Comparative Examples K12 to K16 including an additivealone.

Evaluation Example K2: Evaluation of lifespan characteristics at 4.25 Vand high temperature (45° C.) and DC-IR evaluation (II) afterhigh-temperature lifespan evaluation

High-temperature lifespan characteristics and DC-IRs of the lithiumbatteries of Examples K7 to K12 and Comparative Examples K12 to K16 weremeasured in the same manner as in Evaluation Example K1.

The measurement results are shown in Table K2 below.

TABLE K2 Direct current internal resistance Capacity increase retentionafter high- ratio at temperature 900^(th) lifespan cycle evaluation [%][%] Example K7 78.1 179.9 (SEI-1316 1.0 wt % + OA1300 1.0 wt %) ExampleK8 77.7 172.1 (SEI-1316 1.0 wt % + OA1300 0.25 wt %) Example K9 78.0173.7 (SEI-1316 1.0 wt % + OA1300 0.5 wt %) Example K10 77.2 183.8(SEI-1316 1.0 wt % + OA1300 3.0 wt %) Example K11 77.5 177.5 (SEI-13161.0 wt % + OA1301 1.0 wt %) Example K12 77.3 178.0 (SEI-1316 1.0 wt % +OA1301 0.5 wt %) Comparative Example K17 63.7 208.8 (SEI-1316 1.0 wt % +TEPi 1.0 wt %) Comparative Example K18 65.1 210.5 (SEI-1316 2.0 wt % +TEPi 0.5 wt %) Comparative Example K19 65.3 205.2 (SEI-1316 0 wt % +TEPa 1.0 wt %) Comparative Example K20 64.5 207.4 (SEI-1316 0 wt % +TEPa0.5 wt %) Comparative Example K21 61.8 213.7 (SEI-1316 0 wt % +TFEP 1.0wt %) Comparative Example K22 62.1 211.2 (SEI-1316 0 wt % + TFEP 0.5 wt%)

As shown in Table K2, the lithium batteries of Examples K7 to K12including the cyclic phosphate-based additives of the present disclosureexhibited enhanced high-temperature lifespan characteristics, ascompared to the lithium batteries of Comparative Examples K17 to K22including acyclic phosphate-based additives. In addition, the lithiumbatteries of Examples K7 to K12 including the cyclic phosphate-basedadditives of the present disclosure exhibited lower direct currentinternal resistance increases, as compared to the lithium batteries ofComparative Examples K17 to K22 including acyclic phosphate-basedadditives.

Evaluation Example K3: High-Temperature (45° C.) Stability Evaluationand DC-IR Evaluation after High-Temperature Storage

High-temperature stability of each of the lithium batteries manufacturedaccording to Examples K7 to K12 and Comparative Examples K12 to K22 wasevaluated using the following method.

The lithium batteries of Examples K7 to K12 and Comparative Examples K12to K22 were subjected to the 1^(st) cycle of charging and discharging asfollows. Each lithium battery was charged at a constant current of 0.5 Crate at 25° C. until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.5 C rate until the voltage reached 2.8 V.

Each lithium battery was subjected to the 2^(nd) cycle of charging anddischarging as follows. Each lithium battery was charged at a constantcurrent of 0.5 C rate until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.2 C rate until the voltage reached 2.8 V.

Each lithium battery was subjected to the 3^(rd) cycle of charging anddischarging as follows. Each lithium battery was charged at a constantcurrent of 0.5 C rate until the voltage reached 4.3 V and then, whilemaintaining a constant voltage of 4.3 V, each lithium battery wascharged until the current reached 0.05 C and then discharged at aconstant current of 0.2 C rate until the voltage reached 2.80 V. Adischarge capacity at the 3^(rd) cycle was regarded as a standardcapacity.

Each lithium battery was subjected to the 4^(th) cycle of charging anddischarging as follows. Each lithium battery was charged at 0.5 C rateuntil the voltage reached 4.30 V and then, while maintaining a constantvoltage of 4.30 V, each lithium battery was charged until the currentreached 0.05 C, the charged battery was stored in an oven at 60° C. for120 days, and then the battery was taken out of the oven and thendischarged at 0.1 C rate until the voltage reached 2.80 V.

The charging/discharging evaluation results are shown in Table K3 below.A capacity retention ratio after high-temperature storage is definedusing Equation K3 below:

Capacity retention ratio after high-temperature storage [%]=[dischargecapacity at high temperature at 4^(th) cycle/standard capacity]×100(herein, the standard capacity is a discharge capacity at 3^(rd)cycle)  Equation K3

DC-IRs of the lithium batteries of Examples K7 to K12 and ComparativeExamples K12 to K22 and the batteries thereof after storage in an ovenat 60° C. for 120 days and being taken out of the oven were measuredusing the following method.

In the 1^(st) cycle, each lithium battery was charged at a current of0.5 C until the voltage reached 50% SOC (state of charge), followed byresting for 10 minutes, and was discharged at a constant current of 1.0C for 30 minutes.

The current applied during discharging for 30 seconds and the voltageafter discharging were measured, and DC-IR was calculated therefrom.

Initial direct current resistances of the lithium batteries manufacturedaccording to Examples K7 to K12 and Comparative Examples K12 to K16 weremeasured.

Direct current resistances of the lithium batteries after storage in anoven at 60° C. for 120 days were measured.

A part of direct current resistance increases calculated from themeasured initial direct current resistances and the direct currentresistances after high-temperature storage is shown in Table K3 below. Adirect current resistance increase is represented by Equation K4 below.

Direct current resistance increase [%]=[direct current resistance afterhigh-temperature storage/initial direct currentresistance]×100  Equation K4

TABLE K3 Direct current internal Capacity resistance retention increaseratio after high- after high- temperature temperature storage storage[%] [%] Example K7 86.3 151.9 (SEI-1316 1.0 wt % + OA1300 1.0 wt %)Example K8 86.0 154.2 (SEI-1316 1.0 wt % + OA1300 0.25 wt %) Example K986.2 153.5 (SEI-1316 1.0 wt % + OA1300 0.5 wt %) Example K10 86.3 158.8(SEI-1316 1.0 wt % + OA1300 3.0 wt %) Example K11 86.2 152.3 (SEI-13161.0 wt % + OA1301 1.0 wt %) Example K12 86.2 153.1 (SEI-1316 1.0 wt % +OA1301 0.5 wt %) Comparative Example K12 83.2 166.1 (SEI-1316 1.0 wt % +OA1300 0 wt %) Comparative Example K13 81.4 167.8 (SEI-1316 2.0 wt % +OA1300 0 wt %) Comparative Example K14 82.9 169.9 (SEI-1316 0 wt % +OA1300 1.0 wt %) Comparative Example K15 83.1 164.5 (SEI-1316 0 wt % +OA1300 0.5 wt %) Comparative Example K16 82.8 172.5 (SEI-1316 0 wt % +OA1300 3.0 wt %) Comparative Example K17 81.5 180.7 (SEI-1316 1.0 wt % +TEPi 1.0 wt %) Comparative Example K18 81.3 182.8 (SEI-1316 2.0 wt % +TEPi 0.5 wt %) Comparative Example K19 80.4 176.9 (SEI-1316 0 wt % +TEPa 1.0 wt %) Comparative Example K20 79.5 175.5 (SEI-1316 0 wt % +TEPa 0.5 wt %) Comparative Example K21 79.5 179.2 (SEI-1316 0 wt % +TFEP 1.0 wt %) Comparative Example K22 80.2 177.3 (SEI-1316 0 wt % +TFEP 0.5 wt %)

As shown in Table K3, the lithium batteries of Examples K7 to K12simultaneously including two additives of the present disclosureexhibited enhanced lifespan characteristics after high-temperaturestorage, as compared to the lithium batteries of Comparative ExamplesK12 to K16 including an additive alone.

The lithium batteries of Examples K7 to K12 simultaneously including twoadditives of the present disclosure exhibited lower direct currentinternal resistance increases after high-temperature storage, ascompared to the lithium batteries of Comparative Examples K12 to K16including an additive alone.

The batteries of Examples K7 to K12 including the cyclic phosphate-basedadditives of the present disclosure exhibited enhanced lifespancharacteristics after high-temperature storage, as compared to thelithium batteries of Comparative Examples K17 to K22 including acyclicphosphate-based additives.

In addition, the lithium batteries of Examples K7 to K12 including thecyclic phosphate-based additives of the present disclosure exhibitedlower direct current internal resistance increases afterhigh-temperature storage, as compared to the lithium batteries ofComparative Examples K17 to K22 including acyclic phosphate-basedadditives.

Evaluation Example K4: Gas Generation Evaluation after High-TemperatureStorage

The initial thicknesses of the lithium batteries of Examples K7 to K12and Comparative Examples K12 to K22 were measured using a micrometer.

Subsequently, each of the manufactured batteries was stored in an ovenat 60° C. for 63 days, and then taken out of the oven, followed bycooling at room temperature for 4 hours or greater, and the thickness ofeach lithium battery was measured again.

Thickness increases calculated from the measured initial thicknesses andthicknesses after high-temperature (60° C.) storage are shown in TableK4 below. A thickness increase is represented by Equation K5 below:

Thickness increase [%]=[Thickness of lithium battery afterhigh-temperature storage/initial thickness of lithiumbattery]×100  Equation K5

TABLE K4 Thickness increase after high- temperature storage [%] ExampleK7 127.7 (SEI-1316 1.0 wt % + OA1300 1.0 wt %) Example K8 135.6(SEI-1316 1.0 wt % + OA1300 0.25 wt %) Example K9 132.1 (SEI-1316 1.0 wt% + OA1300 0.5 wt %) Example K10 120.1 (SEI-1316 1.0 wt % + OA1300 3.0wt %) Example K11 133.4 (SEI-1316 1.0 wt % + OA1301 1.0 wt %) ExampleK12 137.5 (SEI-1316 1.0 wt % + OA1301 0.5 wt %) Comparative Example K12165.1 (SEI-1316 1.0 wt % + OA1300 0 wt %) Comparative Example K13 164.3(SEI-1316 2.0 wt % + OA1300 0 wt %) Comparative Example K14 153.1(SEI-1316 0 wt % + OA1300 1.0 wt %) Comparative Example K15 157.7(SEI-1316 0 wt % + OA1300 0.5 wt %) Comparative Example K16 149.4(SEI-1316 0 wt % + OA1300 3.0 wt %) Comparative Example K17 172.2(SEI-1316 1.0 wt % + TEPi 1.0 wt %) Comparative Example K18 171.7(SEI-1316 2.0 wt % + TEPi 0.5 wt %) Comparative Example K19 165.5(SEI-1316 0 wt % + TEPa 1.0 wt %) Comparative Example K20 165.3(SEI-1316 0 wt % + TEPa 0.5 wt %) Comparative Example K21 160.5(SEI-1316 0 wt % + TFEP 1.0 wt %) Comparative Example K22 160.3(SEI-1316 0 wt % + TFEP 0.5 wt %)

As shown in Table K3, the lithium batteries of Examples K7 to K12simultaneously including two additives of the present disclosureexhibited lower thickness increases after high-temperature storage, ascompared to the lithium batteries of Comparative Examples K12 to K16including an additive alone. Thus, gas generation at high temperaturewas suppressed.

The lithium batteries of Examples K7 to K12 including the cyclicphosphate-based additives of the present disclosure exhibited lowerthickness increases after high-temperature storage, as compared to thelithium batteries of Comparative Examples K17 to K22 including acyclicphosphate-based additives.

Evaluation Example K5: Evaluation of Electrochemical Stability ofElectrolytic Solution

An electrochemical cell was prepared using copper foil as a workingelectrode, lithium foil as a counter electrode, and each of the organicelectrolytic solutions prepared according to Example K1 and ComparativeExample K1 as an electrolytic solution.

Each electrochemical cell was stored in an oven at 60° C. for 2 hours,and then taken out and left at room temperature for 30 days to evaluatethe appearance.

The electrochemical cell including the organic electrolytic solution ofExample K1 maintained a colorless and transparent color, whereas theelectrochemical cell including the organic electrolytic solution ofComparative Example K1 turned brown.

Thus, it may be seen that the organic electrolytic solution of ExampleK1 simultaneously including two additives exhibited enhanced thermalstability through the prevention of side reactions in the organicelectrolytic solution, as compared to the organic electrolytic solutionof Comparative Example K1 including an additive alone.

As is apparent from the foregoing description, a lithium batteryincluding an organic electrolytic solution including both a novelbicyclic sulfate-based additive and a monocyclic phosphate-basedadditive may exhibit enhanced high-temperature characteristics andlifespan characteristics.

By way of summation and review, when lithium batteries operate at highoperating voltages, aqueous electrolytic solutions highly reactive tolithium may not be suitable for use in such lithium batteries. Lithiumbatteries generally use organic electrolytic solutions. An organicelectrolytic solution is prepared by dissolving a lithium salt in anorganic solvent. An organic solvent with stability at high voltages,high ionic conductivity, high dielectric constant, and low viscosity maybe used.

When a lithium battery uses a general organic electrolytic solutionincluding a carbonate-based polar non-aqueous solvent, an irreversiblereaction, in which charges are excessively used due to a side reactionbetween the anode/cathode and the organic electrolytic solution, mayoccur during initial charging. As a result of such an irreversiblereaction, a passivation layer, such as a solid electrolyte interface(SEI) layer, may be formed at a surface of an anode. In addition, aprotection layer is formed at a surface of a cathode.

In this regard, the SEI layer and/or the protection layer, formed usingan existing organic electrolytic solution, may be easily degraded. Forexample, such an SEI layer and/or protection layer may exhibit decreasedstability at a high temperature.

Therefore, an organic electrolytic solution capable of forming an SEIlayer and/or a protection layer having improved high-temperaturestability is desirable.

Embodiments provide a lithium battery including a cathode including alithium transition metal oxide having high nickel content and an organicelectrolytic solution including a novel bicyclic sulfate-based additive.The lithium battery according to embodiments exhibits enhancedhigh-temperature characteristics and lifespan characteristics.

Example embodiments have been disclosed herein, and although specificterms are employed, they are used and are to be interpreted in a genericand descriptive sense only and not for purpose of limitation. In someinstances, as would be apparent to one of ordinary skill in the art asof the filing of the present application, features, characteristics,and/or elements described in connection with a particular embodiment maybe used singly or in combination with features, characteristics, and/orelements described in connection with other embodiments unless otherwisespecifically indicated. Accordingly, it will be understood by those ofskill in the art that various changes in form and details may be madewithout departing from the spirit and scope of the present invention asset forth in the following claims.

What is claimed is:
 1. An organic electrolytic solution, comprising: afirst lithium salt; an organic solvent; a bicyclic sulfate-basedcompound represented by Formula 1 below; and a monocyclicphosphate-based compound represented by Formula K1 below:

wherein: in Formula 1, each of A₁, A₂, A₃, and A₄ is independently acovalent bond, a substituted or unsubstituted C₁-C₅ alkylene group, acarbonyl group, or a sulfinyl group, wherein both A₁ and A₂ are not acovalent bond and both A₃ and A₄ are not a covalent bond, and in FormulaK1, each of A₅ and A₆ is independently a substituted or unsubstitutedC₁-C₅ alkylene group.
 2. The organic electrolytic solution as claimed inclaim 1, wherein at least one of A₁, A₂, A₃, and A₄ is an unsubstitutedor substituted C₁-C₅ alkylene group, wherein a substituent of thesubstituted C₁-C₅ alkylene group is at least one selected from ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom, and at least one of A₅and A₆ is an unsubstituted or substituted C₁-C₅ alkylene group, whereina substituent of the substituted C₁-C₅ alkylene group is ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, or a polarfunctional group having at least one heteroatom.
 3. The organicelectrolytic solution as claimed in claim 1, wherein at least one of A₁,A₂, A₃, and A₄ is an unsubstituted or substituted C₁-C₅ alkylene group,wherein a substituent of the substituted C₁-C₅ alkylene group is ahalogen, a methyl group, an ethyl group, a propyl group, an isopropylgroup, a butyl group, a tert-butyl group, a trifluoromethyl group, atetrafluoroethyl group, a phenyl group, a naphthyl group, atetrafluorophenyl group, a pyrrolyl group, or a pyridinyl group, and atleast one of A₅ and A₆ is a substituted C₁-C₅ alkylene group, wherein asubstituent of the substituted C₁-C₅ alkylene group is a halogen, amethyl group, an ethyl group, a propyl group, an isopropyl group, abutyl group, a tert-butyl group, a monofluoromethyl group, adifluoromethyl group, a trifluoromethyl group, or a tetrafluoroethylgroup.
 4. The organic electrolytic solution as claimed in claim 2,wherein the substituted C₁-C₅ alkylene group is substituted with a polarfunctional group including at least one heteroatom, wherein the polarfunctional group is —F, —Cl, —Br, —I, —CN, —N═C═S, —(CH₂CH₂O)_(n)—R¹² (nis an integer of 1 to 10), —C(═O)OR¹⁶, —OR¹⁶, —OC(═O)OR¹⁶,—R¹⁵OC(═O)OR¹⁶, —C(═O)R¹⁶, —R¹⁵C(═O)R¹⁶, —OC(═O)R¹⁶, —R¹⁵OC(═O)R¹⁶,—C(═O)—O—C(═O)R¹⁶, —R¹⁵C(═O)—O—C(═O)R¹⁶, —SR¹⁶, —R¹⁵SR¹⁶, —SSR¹⁶,—R¹⁵SSR¹⁶, —S(═O)R¹⁶, —R¹⁵S(═O)R¹⁶, —R¹⁵C(═S)R¹⁶, —R¹⁵C(═S)SR¹⁶,—R¹⁵SO₃R¹⁶, —SO₃R¹⁶, —NNC(═S)R¹⁶, —R¹⁵NNC(═S)R¹⁶, —R¹⁵N═C═S, —NCO,—R¹⁵—NCO, —NO₂, —R¹⁵NO₂, —R¹⁵SO₂R¹⁶, —SO₂R¹⁶,

wherein, in the formulae above, each of R¹¹ and R¹⁵ is independently ahalogen-substituted or unsubstituted C₁-C₂₀ alkylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenylene group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynylene group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkylene group, ahalogen-substituted or unsubstituted C₆-C₄₀ arylene group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroarylene group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylarylene group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkylene group; and eachof R¹², R¹³, R¹⁴ and R¹⁶ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₁₂ cycloalkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ alkylaryl group, ahalogen-substituted or unsubstituted C₇-C₁₅ trialkylsilyl group, or ahalogen-substituted or unsubstituted C₇-C₁₅ aralkyl group.
 5. Theorganic electrolytic solution as claimed in claim 1, wherein thebicyclic sulfate-based compound represented by Formula 1 is representedby Formula 2 or 3:

wherein, in Formulae 2 and 3, each of B₁, B₂, B₃, B₄, D₁, and D₂ isindependently —C(E₁)(E₂)-, a carbonyl group, or a sulfinyl group; andeach of E₁ and E₂ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkenyl group, ahalogen-substituted or unsubstituted C₂-C₂₀ alkynyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ cycloalkenyl group, ahalogen-substituted or unsubstituted C₃-C₂₀ heterocyclic group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.
 6. Theorganic electrolytic solution as claimed in claim 5, wherein each of E₁and E₂ is independently hydrogen, a halogen, a halogen-substituted orunsubstituted C₁-C₁₀ alkyl group, a halogen-substituted or unsubstitutedC₆-C₄₀ aryl group, or a halogen-substituted or unsubstituted C₂-C₄₀heteroaryl group.
 7. The organic electrolytic solution as claimed inclaim 5, wherein each of E₁ and E₂ is independently hydrogen, fluorine(F), chlorine (Cl), bromine (Br), iodine (I), a methyl group, an ethylgroup, a propyl group, an isopropyl group, a butyl group, a tert-butylgroup, a trifluoromethyl group, a tetrafluoroethyl group, a phenylgroup, a naphthyl group, a tetrafluorophenyl group, a pyrrolyl group, ora pyridinyl group.
 8. The organic electrolytic solution as claimed inclaim 1, wherein the bicyclic sulfate-based compound represented byFormula 1 is represented by Formula 4 or 5:

wherein, in Formulae 4 and 5, each of R₁, R₂, R₃, R₄, R₂₁, R₂₂, R₂₃,R₂₄, R₂₅, R₂₆, R₂₇, and R₂₈ is independently hydrogen, a halogen, ahalogen-substituted or unsubstituted C₁-C₂₀ alkyl group, ahalogen-substituted or unsubstituted C₆-C₄₀ aryl group, or ahalogen-substituted or unsubstituted C₂-C₄₀ heteroaryl group.
 9. Theorganic electrolytic solution as claimed in claim 8, wherein each of R₁,R₂, R₃, R₄, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, R₂₇, and R₂s is independentlyhydrogen, F, Cl, Br, I, a methyl group, an ethyl group, a propyl group,an isopropyl group, a butyl group, a tert-butyl group, a trifluoromethylgroup, a tetrafluoroethyl group, a phenyl group, a naphthyl group, atetrafluorophenyl group, a pyrrolyl group, or a pyridinyl group.
 10. Theorganic electrolytic solution as claimed in claim 1, wherein thebicyclic sulfate-based compound represented by Formula 1 is representedby one of Formulae 6 to 17 below:


11. The organic electrolytic solution as claimed in claim 1, wherein:the monocyclic phosphate-based compound represented by Formula K1 isrepresented by Formula K2 below:

in Formula K2, each of R₂₉, R₃₀, R₃₁, and R₃₂ is independently hydrogen,halogen, an unsubstituted or halogen-substituted C₁-C₂₀ alkyl group, ora polar functional group containing a heteroatom, and the polarfunctional group containing a heteroatom is —CN, —N═C═O, —N═C═S,—(CH₂CH₂O)_(n)—CH₃, in which n is an integer of 1 to 10, —OS(═O)₂F,—OS(═O)₂CH₃, —OS(═O)₂CH₂CH₃, or —OS(═O)₂CF₃.
 12. The organicelectrolytic solution as claimed in claim 1, wherein the monocyclicphosphate-based compound represented by Formula K1 is represented by oneof Formulae K3 to K14 below:


13. The organic electrolytic solution as claimed in claim 1, wherein: anamount of the bicyclic sulfate-based compound is from about 0.1 wt % toabout 5 wt %, based on a total weight of the organic electrolyticsolution, and an amount of the monocyclic phosphate-based compound isfrom about 0.05 wt % to about 5 wt %, based on the total weight of theorganic electrolytic solution.
 14. The organic electrolytic solution asclaimed in claim 1, wherein the first lithium salt in the organicelectrolytic solution includes LiPF₆, LiBF₄, LiSbF₆, LiAsF₆, LiClO₄,LiCF₃SO₃, Li(CF₃SO₂)₂N, LiC₄F₉SO₃, LiAlO₂, LiAlCl₄,LiN(C_(x)F_(2x+1)SO₂)(C_(y)F_(2y+1)SO₂) where 2≤x≤20 and 2≤y≤20, LiCl,or LiI.
 15. The organic electrolytic solution as claimed in claim 1,further comprising a cyclic carbonate compound, wherein the cycliccarbonate compound is vinylene carbonate (VC), VC substituted with ahalogen, a cyano (CN) group, or a nitro group (NO₂), vinylethylenecarbonate (VEC), VEC substituted with a halogen, CN, or NO₂,fluoroethylene carbonate (FEC), or FEC substituted with a halogen, CN,or NO₂.
 16. The organic electrolytic solution as claimed in claim 14,wherein an amount of the cyclic carbonate compound is from about 0.01 wt% to about 5 wt %, based on a total weight of the organic electrolyticsolution.
 17. The organic electrolytic solution as claimed in claim 1,further comprising a second lithium salt represented by one of Formulae18 to 25 below:


18. The organic electrolytic solution as claimed in claim 17, wherein anamount of the second lithium salt is from about 0.1 wt % to about 5 wt %based on a total weight of the organic electrolytic solution.
 19. Alithium battery, comprising: a cathode including a cathode activematerial; an anode including an anode active material; and the organicelectrolytic solution according to claim 1 between the cathode and theanode.
 20. The lithium battery as claimed in claim 19, wherein: thecathode active material includes a nickel-containing layered lithiumtransition metal oxide, and a content of nickel in the lithiumtransition metal oxide is about 60 mol % or more with respect to a totalnumber of moles of transition metals.
 21. The lithium battery as claimedin claim 20, wherein: the lithium transition metal oxide is representedby Formula 26 below:Li_(a)Ni_(x)Co_(y)M_(z)O_(2-b)A_(b)  <Formula 26> in Formula 26,1.0≤a≤1.2, 0≤b≤0.2, 0.6≤x<1, 0<y≤0.3, 0<z≤0.3, and x+y+z=1; M ismanganese (Mn), vanadium (V), magnesium (Mg), gallium (Ga), silicon(Si), tungsten (W), molybdenum (Mo), iron (Fe), chromium (Cr), copper(Cu), zinc (Zn), titanium (Ti), aluminum (Al), boron (B), or acombination thereof, and A is fluorine (F), sulfur (S), chlorine (Cl),bromine (Br), or a combination thereof.